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636-94-2 Usage

Uses

2-Hydroxyterephthalic acid is a useful reagent and reactant in the field of nanotechnology, and material science. Della Pia, A., et al.: Faraday Discuss., 204, 191-213 (2017);

General Description

This product has been enhanced for energy efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 636-94-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 636-94:
(5*6)+(4*3)+(3*6)+(2*9)+(1*4)=82
82 % 10 = 2
So 636-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O5/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3,9H,(H,10,11)(H,12,13)

636-94-2 Well-known Company Product Price

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  • Aldrich

  • (752525)  2-Hydroxyterephthalic acid Green Alternative  97%

  • 636-94-2

  • 752525-1G

  • 1,065.87CNY

  • Detail

636-94-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxyterephthalic Acid

1.2 Other means of identification

Product number -
Other names 2-hydroxyterephthalic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:636-94-2 SDS

636-94-2Synthetic route

2,5-dibromoterephtalic acid
13731-82-3

2,5-dibromoterephtalic acid

A

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

B

2,5-dihydroxy-1,4-benzenedicarboxylic acid
610-92-4

2,5-dihydroxy-1,4-benzenedicarboxylic acid

Conditions
ConditionsYield
Stage #1: 2,5-dibromoterephtalic acid With sodium carbonate In water for 1h; Heating / reflux;
Stage #2: With water; 2,2,6,6-tetramethylheptane-3,5-dione; copper(I) bromide at 80℃; for 30h;
Stage #3: With hydrogenchloride In water at 25℃;
A n/a
B 92%
2-bromo-1,4-benzenedicarboxylic acid
586-35-6

2-bromo-1,4-benzenedicarboxylic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With sodium hydroxide; sodium acetate; copper In water for 72h; Heating;99%
With sodium hydroxide; sodium acetate; copper In water for 80h; Heating;99%
With sodium acetate; copper; sodium hydroxide In water for 72h; Reflux;99%
3-aminoterephthalic acid
10312-55-7

3-aminoterephthalic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
Stage #1: 3-aminoterephthalic acid With sodium hydroxide In water
Stage #2: With hydrogenchloride; sodium nitrite In water at 10 - 15℃;
Stage #3: With water; copper(II) sulfate at 15 - 85℃; for 12h;
85%
With potassium nitrite; sulfuric acid Diazotization;
Stage #1: 3-aminoterephthalic acid With hydrogenchloride; sodium hydroxide; sodium nitrite In water at 10℃; for 4h;
Stage #2: With copper(II) sulfate at 85℃; for 12h;
terephthalic acid
100-21-0

terephthalic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With photocatalytic titania-coated hollow glass microspheres In water Irradiation;35%
With sodium phosphate buffer; dihydrogen peroxide; copper(II) sulfate In water Kinetics; Further Variations:; Reagents; OH radical generation without/with irradiation; Oxidation;
Multi-step reaction with 3 steps
1: HNO3+H2SO4
2: tin; hydrochloric acid
3: potassium nitrite; sulfuric acid / Diazotization
View Scheme
terephthalic acid
100-21-0

terephthalic acid

sodium hydroxide
1310-73-2

sodium hydroxide

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With Fe3O4/C/ZnO core-shell composite; CR dye In water for 0.166667h; Irradiation;
With zinc(II) oxide In water Reagent/catalyst; UV-irradiation;
1,2-dihydroxycyclohexa-3,5-diene-1,4-dicarboxylic acid

1,2-dihydroxycyclohexa-3,5-diene-1,4-dicarboxylic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
In sodium hydroxide; sulfuric acid
carbon dioxide
124-38-9

carbon dioxide

3-Trifluoromethylphenol
98-17-9

3-Trifluoromethylphenol

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With potassium carbonate at 300℃;
dimethyl aminoterephthalate
5372-81-6

dimethyl aminoterephthalate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
Stage #1: dimethyl aminoterephthalate With sulfuric acid; sodium nitrite at 0℃; for 0.5h;
Stage #2: With sulfuric acid at 120℃; for 0.333333h; Sandmeyer reaction; Further stages.;
66.5%
4-trifluoromethylsalicylic acid
328-90-5

4-trifluoromethylsalicylic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With sulfuric acid
In various solvent(s) Irradiation;
3-Trifluoromethylphenol
98-17-9

3-Trifluoromethylphenol

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: K2CO3
2: H2SO4
View Scheme
2-monochlorophenol
95-57-8

2-monochlorophenol

A

glutaconic acid
1724-02-3

glutaconic acid

B

ortoquinone
583-63-1

ortoquinone

C

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

D

oxalic acid
144-62-7

oxalic acid

E

benzene-1,2-diol
120-80-9

benzene-1,2-diol

F

maleic acid
110-16-7

maleic acid

G

phenol
108-95-2

phenol

Conditions
ConditionsYield
With sodium sulfate at 30℃; Kinetics; Reagent/catalyst; Electrolysis;
terephthalic acid
100-21-0

terephthalic acid

A

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

B

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

Conditions
ConditionsYield
With titanium(IV) dioxide Kinetics; Reagent/catalyst; UV-irradiation;
p-Toluic acid
99-94-5

p-Toluic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With phosphorus pentaoxide; sulfuric acid at 250℃; im Rohr; durch Verschmelzen des Reaktionsprodukts mit Kaliumhydroxyd;
2-hydroxy-4-hydroxymethyl-benzaldehyde

2-hydroxy-4-hydroxymethyl-benzaldehyde

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With potassium hydroxide at 220℃;
2-isopropyl-5-methylphenoxyacetic acid
5333-40-4

2-isopropyl-5-methylphenoxyacetic acid

A

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

B

3-Carboxyphenol
99-06-9

3-Carboxyphenol

Conditions
ConditionsYield
With sodium hydroxide at 240 - 250℃;
2,5-Dimethylphenol
95-87-4

2,5-Dimethylphenol

A

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

B

2-hydroxy-p-toluic acid
50-85-1

2-hydroxy-p-toluic acid

Conditions
ConditionsYield
With potassium carbonate beim Schmelzen;
With potassium hydroxide
2-methoxyterephthalic acid
5156-00-3

2-methoxyterephthalic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With hydrogenchloride unter Druck;
With potassium carbonate durch Schmelzen;
methyl 4-cyano-3-hydroxybenzoate
6520-87-2

methyl 4-cyano-3-hydroxybenzoate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With sulfuric acid
hydroxy-terephthalic acid diethyl ester
74744-72-2

hydroxy-terephthalic acid diethyl ester

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With alkaline solution
2-nitroterephthalic acid
610-29-7

2-nitroterephthalic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: tin; hydrochloric acid
2: potassium nitrite; sulfuric acid / Diazotization
View Scheme
3-bromo-4-methylbenzoic acid
7697-26-9

3-bromo-4-methylbenzoic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: permanganate
2: sodium hydroxide
View Scheme
methyl 4-methyl-2-methoxybenzoate
81245-24-1

methyl 4-methyl-2-methoxybenzoate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: alcoholic potash
2: KMnO4; diluted alkali
3: potash / durch Schmelzen
View Scheme
2-methoxy-4-methylbenzoic acid
704-45-0

2-methoxy-4-methylbenzoic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: KMnO4; diluted alkali
2: potash / durch Schmelzen
View Scheme
oxyterephthalic acid monoethyl ester

oxyterephthalic acid monoethyl ester

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

congo red
14684-01-6

congo red

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
With cadmium ferrite; water at 100℃; for 0.166667h; pH=7; Kinetics; Catalytic behavior; pH-value; Microwave irradiation;
4-methyl-benzoic acid sulfamide-(3)

4-methyl-benzoic acid sulfamide-(3)

A

3-hydroxy-4-methylbenzoic acid
586-30-1

3-hydroxy-4-methylbenzoic acid

B

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
bei der Kalischmelze;
thymol
89-83-8

thymol

A

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

B

3-oxy-benzoic acid ; 3-oxy-4-isopropyl-benzoic acid

3-oxy-benzoic acid ; 3-oxy-4-isopropyl-benzoic acid

Conditions
ConditionsYield
bei der Kalischmelze;
carvacrol
499-75-2

carvacrol

A

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

B

4-isopropyl-2-hydroxybenzoic acid
20154-41-0

4-isopropyl-2-hydroxybenzoic acid

hydrogenchloride
7647-01-0

hydrogenchloride

2-methoxyterephthalic acid
5156-00-3

2-methoxyterephthalic acid

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Conditions
ConditionsYield
at 160℃;
2-isopropyl-5-methylphenoxyacetic acid
5333-40-4

2-isopropyl-5-methylphenoxyacetic acid

alkali

alkali

A

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

B

3-hydroxy-4-isopropyl-benzoic acid
19420-59-8

3-hydroxy-4-isopropyl-benzoic acid

C

3-Carboxyphenol
99-06-9

3-Carboxyphenol

Conditions
ConditionsYield
at 240 - 250℃;
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

water
7732-18-5

water

zirconium(IV) chloride
10026-11-6

zirconium(IV) chloride

acetic acid
64-19-7

acetic acid

5.6C8H4O5(2-)*4HO(1-)*4O(2-)*6Zr(4+)*0.8C2H3O2(1-)

5.6C8H4O5(2-)*4HO(1-)*4O(2-)*6Zr(4+)*0.8C2H3O2(1-)

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 120℃; for 24h; Reagent/catalyst;99%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

(3S,4S)-N3,N4-bis(((1S,2R)-2-phenylcyclopropyl)carbamoyl)pyrrolidine-3,4-dicarboxamide hydrochloride

(3S,4S)-N3,N4-bis(((1S,2R)-2-phenylcyclopropyl)carbamoyl)pyrrolidine-3,4-dicarboxamide hydrochloride

(3S,3’S,4S,4’S)-1,1’-(2-hydroxyterephthaloyl)-bis(N3,N4-bis((1S,2R)-2-phenylcyclopropyl)pyrrolidine-3,4-dicarboxamide)

(3S,3’S,4S,4’S)-1,1’-(2-hydroxyterephthaloyl)-bis(N3,N4-bis((1S,2R)-2-phenylcyclopropyl)pyrrolidine-3,4-dicarboxamide)

Conditions
ConditionsYield
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 23℃; for 18h;98%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

2-hydroxyterephthaloyl dichloride

2-hydroxyterephthaloyl dichloride

Conditions
ConditionsYield
With thionyl chloride; N,N-dimethyl-formamide at 90℃; for 48h; Inert atmosphere;97%
With thionyl chloride
With thionyl chloride; N,N-dimethyl-formamide for 3h; Heating;
With thionyl chloride; N,N-dimethyl-formamide In dichloromethane at 20 - 45℃; Inert atmosphere;
methanol
67-56-1

methanol

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

dimethyl hydroxyterephthalate
6342-72-9

dimethyl hydroxyterephthalate

Conditions
ConditionsYield
With sulfuric acid for 18h; Reflux;95%
With thionyl chloride for 21h; Concentration; Reflux;94.16%
With thionyl chloride at 0 - 85℃; for 2.5h; Inert atmosphere;90%
lead(II) nitrate

lead(II) nitrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

2-(2-carboxylphenyl)-imidazo[4,5-f ]-1,10-phenanthroline
552843-44-4

2-(2-carboxylphenyl)-imidazo[4,5-f ]-1,10-phenanthroline

[Pb2(2-(2-carboxyphenyl)imidazo(4,5-f )-(1,10)phenanthroline)2(2-hydroxy-1,4-benzenedicarboxylic acid)]n

[Pb2(2-(2-carboxyphenyl)imidazo(4,5-f )-(1,10)phenanthroline)2(2-hydroxy-1,4-benzenedicarboxylic acid)]n

Conditions
ConditionsYield
With sodium hydroxide In water at 169.84℃; for 72h; pH=8; Autoclave;90%
3(5)-amino-1,2,4-triazole
61-82-5

3(5)-amino-1,2,4-triazole

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

cobalt(II) diacetate tetrahydrate
6147-53-1

cobalt(II) diacetate tetrahydrate

indium(III) chloride
10025-82-8

indium(III) chloride

[In3O(hbdc)3][Co2(atrz)3(H2O)4Cl2]

[In3O(hbdc)3][Co2(atrz)3(H2O)4Cl2]

Conditions
ConditionsYield
With hydrogenchloride In water; N,N-dimethyl-formamide at 100℃; for 96h; Sealed tube;87%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

(3S,4S)-N3,N4-bis(4-fluorophenethyl)pyrrolidine-3,4-dicarboxamide hydrochloride

(3S,4S)-N3,N4-bis(4-fluorophenethyl)pyrrolidine-3,4-dicarboxamide hydrochloride

(3S,3’S,4S,4’S)-1,1’-(2-hydroxyterephthaloyl)-bis(N3,N4-bis(4-fluorophenethyl)pyrrolidine-3,4-dicarboxamide)

(3S,3’S,4S,4’S)-1,1’-(2-hydroxyterephthaloyl)-bis(N3,N4-bis(4-fluorophenethyl)pyrrolidine-3,4-dicarboxamide)

Conditions
ConditionsYield
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 23℃;87%
1,2,4-Triazole
288-88-0

1,2,4-Triazole

iron(III) chloride hexahydrate

iron(III) chloride hexahydrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

[Fe3O(hbdc)3][Fe2(trz)3(H2O)4Cl2]

[Fe3O(hbdc)3][Fe2(trz)3(H2O)4Cl2]

Conditions
ConditionsYield
With trifluoroacetic acid In N,N-dimethyl-formamide at 150℃; for 24h; Reagent/catalyst; Autoclave;85%
1,2,4-Triazole
288-88-0

1,2,4-Triazole

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

cobalt(II) diacetate tetrahydrate
6147-53-1

cobalt(II) diacetate tetrahydrate

indium(III) chloride
10025-82-8

indium(III) chloride

[In3O(bdc)3][Co2(datrz)3(H2O)4Cl2]

[In3O(bdc)3][Co2(datrz)3(H2O)4Cl2]

Conditions
ConditionsYield
In water; N,N-dimethyl-formamide at 120℃; for 48h; Sealed tube;84%
1,2,4-Triazole
288-88-0

1,2,4-Triazole

iron(III) chloride hexahydrate

iron(III) chloride hexahydrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

magnesium(II) acetate tetrahydrate
16674-78-5

magnesium(II) acetate tetrahydrate

[Fe3O(hbdc)3][Mg2(trz)3(H2O)4Cl2]

[Fe3O(hbdc)3][Mg2(trz)3(H2O)4Cl2]

Conditions
ConditionsYield
With trifluoroacetic acid In N,N-dimethyl-formamide at 150℃; for 24h; Autoclave;83%
N-formyldiethylamine
617-84-5

N-formyldiethylamine

copper nitrate hemi(pentahydrate)

copper nitrate hemi(pentahydrate)

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

(2-hydroxybenzene-1,4-dicarboxylate)aquacopper(II) - diethylformamide (2/1)

(2-hydroxybenzene-1,4-dicarboxylate)aquacopper(II) - diethylformamide (2/1)

Conditions
ConditionsYield
In ethanol High Pressure; Cu salt amd ligand (1.2:1) dissolved in DEF/EtOH (8:3 v/v), sealed, heated at 65°C for 24 h; washed (EtOH) several times;81.1%
1,3,5-tris(1-imidazolyl)benzene

1,3,5-tris(1-imidazolyl)benzene

zinc(II) sulfate heptahydrate

zinc(II) sulfate heptahydrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

2C8H5O5(1-)*2C15H12N6*C8H4O5(2-)*2H2O*2Zn(2+)

2C8H5O5(1-)*2C15H12N6*C8H4O5(2-)*2H2O*2Zn(2+)

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 85℃; for 72h; Autoclave; High pressure;78%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

2-chloro-ethanol
107-07-3

2-chloro-ethanol

2-(2'-hydroxyethoxy)terephthalic acid
111822-80-1

2-(2'-hydroxyethoxy)terephthalic acid

Conditions
ConditionsYield
With sodium hydroxide In water for 48h; Ambient temperature;76%
aluminum(III) nitrate nonahydrate

aluminum(III) nitrate nonahydrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

Al(3+)*HO(1-)*C8H4O5(2-)

Al(3+)*HO(1-)*C8H4O5(2-)

Conditions
ConditionsYield
In water; N,N-dimethyl-formamide at 90℃; for 36h;76%
1,3,5-tris(1-imidazolyl)benzene

1,3,5-tris(1-imidazolyl)benzene

cadmium(II) carbonate
739319-89-2

cadmium(II) carbonate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

water
7732-18-5

water

[Cd(1,3,5-tris(1-imidazolyl)benzene)(2-OH-1,4-benzenedicarboxylate)]*H2O

[Cd(1,3,5-tris(1-imidazolyl)benzene)(2-OH-1,4-benzenedicarboxylate)]*H2O

Conditions
ConditionsYield
In N,N-dimethyl acetamide at 85℃; for 72h; Autoclave;75%
1,2,4-Triazole
288-88-0

1,2,4-Triazole

iron(III) chloride hexahydrate

iron(III) chloride hexahydrate

nickel(II) nitrate hexahydrate

nickel(II) nitrate hexahydrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

[Fe3O(hbdc)3][Ni2(trz)3(H2O)4Cl2]

[Fe3O(hbdc)3][Ni2(trz)3(H2O)4Cl2]

Conditions
ConditionsYield
With trifluoroacetic acid In N,N-dimethyl-formamide at 150℃; for 24h; Reagent/catalyst; Autoclave;75%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

C14H19BBrClN2O4

C14H19BBrClN2O4

C22H21BBrClN2O7

C22H21BBrClN2O7

Conditions
ConditionsYield
In tert-butyl methyl ether at 20℃;73.2%
titanium(IV) isopropylate
546-68-9

titanium(IV) isopropylate

zinc(II) nitrate hexahydrate

zinc(II) nitrate hexahydrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

[dimethylammonium][Zn3(OH)Ti(2-hydroxyterephthalic acid(-3H))3(HCO2)]*H2O

[dimethylammonium][Zn3(OH)Ti(2-hydroxyterephthalic acid(-3H))3(HCO2)]*H2O

Conditions
ConditionsYield
at 20 - 120℃; for 80h; High pressure;72%
cadmium(II) nitrate tetrhydrate

cadmium(II) nitrate tetrhydrate

1,3,5-tris(1H-tetrazol-5-yl)benzene
193614-99-2

1,3,5-tris(1H-tetrazol-5-yl)benzene

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

[Cd4(OH-BDC)3(HBTT)(N,N-dimethylformamide)2]n

[Cd4(OH-BDC)3(HBTT)(N,N-dimethylformamide)2]n

Conditions
ConditionsYield
In water; dimethyl sulfoxide at 120℃; for 72h;72%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

2-hydroxy-5-chloro-aniline
95-85-2

2-hydroxy-5-chloro-aniline

2,5-bis(5-chloro-2-benzoxazolyl)phenol

2,5-bis(5-chloro-2-benzoxazolyl)phenol

Conditions
ConditionsYield
With PPA at 200℃; for 22h;70%
methanol
67-56-1

methanol

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

C9H7ClO4

C9H7ClO4

Conditions
ConditionsYield
With thionyl chloride for 0.5h; Reflux;69.3%
2-amino-4-ethylphenol
94109-11-2

2-amino-4-ethylphenol

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

2,5-bis(5-ethyl-2-benzoxazolyl)phenol

2,5-bis(5-ethyl-2-benzoxazolyl)phenol

Conditions
ConditionsYield
With PPA at 200℃; for 22h;69%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

terbium nitrate hexahydrate

terbium nitrate hexahydrate

water
7732-18-5

water

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

6Tb(3+)*8HO(1-)*5C8H4O5(2-)*6H2O*7C3H7NO*2C2H7N*C8H6O5

6Tb(3+)*8HO(1-)*5C8H4O5(2-)*6H2O*7C3H7NO*2C2H7N*C8H6O5

Conditions
ConditionsYield
With nitric acid; o-fluoro-benzoic acid at 110℃; for 60h;67%
1,4-diaza-bicyclo[2.2.2]octane
280-57-9

1,4-diaza-bicyclo[2.2.2]octane

zinc(II) nitrate hexahydrate

zinc(II) nitrate hexahydrate

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

Zn(2-hydroxybenzene-1,4-dicarboxylate)(1,4-diazabicyclo[2.2.2]octane)0.5*2DMF*H2O

Zn(2-hydroxybenzene-1,4-dicarboxylate)(1,4-diazabicyclo[2.2.2]octane)0.5*2DMF*H2O

Conditions
ConditionsYield
In N,N-dimethyl-formamide High Pressure; DABCO (0.5 mmol) added to DMF soln. of Zn(NO3)2*6H2O (1.0 mmol) and 2-hydroxybenzene-1,4-dicarboxylic acid (1.0 mmol), heated in screw-capped vial at 110°C for 24 h; cooled, filtered, washed with DMF; elem. anal., XRD;66.9%
2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

europium nitrate hexahydrate

europium nitrate hexahydrate

water
7732-18-5

water

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

6Eu(3+)*8HO(1-)*5C8H4O5(2-)*6H2O*7C3H7NO*2C2H7N*C8H6O5

6Eu(3+)*8HO(1-)*5C8H4O5(2-)*6H2O*7C3H7NO*2C2H7N*C8H6O5

Conditions
ConditionsYield
With nitric acid; o-fluoro-benzoic acid at 110℃; for 48h;65%
ethanol
64-17-5

ethanol

2-hydroxyterephthalic acid
636-94-2

2-hydroxyterephthalic acid

hydroxy-terephthalic acid diethyl ester
74744-72-2

hydroxy-terephthalic acid diethyl ester

Conditions
ConditionsYield
With sulfuric acid at 80℃; for 48h;63%
With toluene-4-sulfonic acid

636-94-2Relevant articles and documents

The influence of different coordination environments on one-dimensional Cu(II) coordination polymers for the photo-degradation of organic dyes

Hussain, Navid,Bhardwaj, Vimal K.

, p. 7697 - 7707 (2016)

Three new Cu(ii) coordination polymers, namely, {[Cu3(L1)(NO3)2(DMF)(H2O)]·3(DMF)}n (1), [Cu3(L1)(Cl)2(DMF)2]n (2) and [Cu3(L2)(NO3)4(H2O)4]n (3), were synthesized from pyridine-2,6-dicarbohydrazide based imine linked tritopic ligands. All the complexes were characterized using elemental analysis, IR, UV-vis spectroscopy and ESI-MS. The solid state structures of complexes 1-3 were determined using single crystal X-ray crystallography. The complexes contain trinuclear copper units connected through different anions that lead to the formation of one dimensional (ID) chain structures. Depending upon the anion of the copper salt and donor atoms of the ligands used in complexation, a small variation in the structures was observed. In complex 1, the trinuclear copper units are connected by phenoxo-bridging (μ2-O-) along with one coordinated water molecule, whereas complex 2 is connected through chloride bridging (μ2-Cl) and complex 3 is connected through nitrate ions (μ-[O-N-O]) along with four water molecules. Photo-catalytic activities of the synthesized complexes (1-3) were investigated. All the complexes were found to be photo-catalytically active; however, the distinct coordination environment of the metal ions (i.e. difference in the coordinated water molecules and donor sites of ligands) played a significant role in the catalytic activities. Therefore, this study presents comparative photo-catalytic studies of different coordination environments of metal ions in one-dimensional Cu(ii) coordination polymers. The results provide a potential pathway for the rational design of more efficient photo-catalysts.

Carboxyfullerene decorated titanium dioxide nanomaterials for reactive oxygen species scavenging activities

Yang, Kai-Cheng,Zheng, Jia-Huei,Chen, Yen-Ling,Lee, Kuen-Chan,Cho, Er-Chieh

, p. 53025 - 53033 (2016)

Titanium dioxide nanomaterials offer superior protection for human skin against ultraviolet light. However, some reports have indicated that they might be associated with adverse effects such as cytotoxicity or reactive oxygen species (ROS) under UV-irrad

Improving photocatalytic reduction of 4-nitrophenol over ZrO2-TiO2 by synergistic interaction between methanol and sulfite ions

Guerrero-Araque, Diana,Acevedo-Pe?a, Próspero,Ramírez-Ortega, David,Gómez, Ricardo

, p. 12655 - 12663 (2017)

The effect of two sacrificial agents (methanol and sodium sulfite) on the photocatalytic reduction of 4-nitrophenol employing a ZrO2-TiO2 photocatalyst is reported. The experimental results showed a decrease in the generation of OH r

New insights into fluorinated TiO2 (brookite, anatase and rutile) nanoparticles as efficient photocatalytic redox catalysts

Wang, Yafang,Li, Liping,Huang, Xinsong,Li, Qi,Li, Guangshe

, p. 34302 - 34313 (2015)

The synthesis of anionic-modified nanostructures with specific properties is often hindered by difficulty in tuning the material compositions without sacrificing phase purity and sample uniformity. Here, we present a novel methodology using NH4

Facile Synthesis of Carbon Dots@2D MoS2 Heterostructure with Enhanced Photocatalytic Properties

Li, Ning,Liu, Zhengtang,Liu, Ming,Xue, Chaorui,Chang, Qing,Wang, Huiqi,Li, Ying,Song, Zhenchao,Hu, Shengliang

, p. 5746 - 5752 (2019)

To better utilize carbon dots (CDs) as efficient photocatalysts, an excellent strategy of constructing CDs@MoS2 heterostructure is presented. Here a facile sonication-hydrothermal method is utilized to synthesize CDs@MoS2. Such heter

DNA Photocleavage by Non-innocent Ligand-Based Ru(II) Complexes

Zhang, Yangyang,Zhou, Qianxiong,Zheng, Yue,Li, Ke,Jiang, Guoyu,Hou, Yuanjun,Zhang, Baowen,Wang, Xuesong

, p. 4296 - 4300 (2016)

In this work, we demonstrate for the first time that [Ru(bpy)2(R-OQN)]+ complexes (bpy = 2,2′-bipyridine, R-OQN = 5-chloro-8-oxyquinolate or 5-bromo-8-oxyquinolate) are able to generate hydroxyl radicals and cleave DNA effectively up

Deciphering a Nanocarbon-Based Artificial Peroxidase: Chemical Identification of the Catalytically Active and Substrate-Binding Sites on Graphene Quantum Dots

Sun, Hanjun,Zhao, Andong,Gao, Nan,Li, Kai,Ren, Jinsong,Qu, Xiaogang

, p. 7176 - 7180 (2015)

Abstract The design and construction of efficient artificial enzymes is highly desirable. Recent studies have demonstrated that a series of carbon nanomaterials possess intrinsic peroxidase activity. Among them, graphene quantum dots (GQDs) have a high en

Enhanced Photoexcited Carrier Separation in Oxygen-Doped ZnIn2S4Nanosheets for Hydrogen Evolution

Yang, Wenlong,Zhang, Lei,Xie, Junfeng,Zhang, Xiaodong,Liu, Qinghua,Yao, Tao,Wei, Shiqiang,Zhang, Qun,Xie, Yi

, p. 6716 - 6720 (2016)

Limited by the relatively sluggish charge-carrier separation in semiconductors, the photocatalytic performance is still far below what is expected. Herein, a model of ZnIn2S4(ZIS) nanosheets with oxygen doping is put forward to obtai

Fabrication of ZnO, ZnS, Ag-ZnS, and Au-ZnS microspheres for photocatalytic activities, CO oxidation and 2-hydroxyterephthalic acid synthesis

Choi, Young In,Lee, Seungwon,Kim, Seog K.,Kim, Young-Il,Cho, Dae Won,Khan, Mohammad Mansoob,Sohn, Youngku

, p. 46 - 56 (2016)

This paper reports the synthesis of ZnS microspheres with cubic and hexagonal crystal phases using a solvothermal method. These materials were characterized by a range of techniques. The effects of Au and Ag-doping on ZnS were also examined. Hexagonal phase ZnO microspheres could be obtained by a CO oxidation process over the ZnS microspheres. The onset of CO oxidation occurred above 350 °C, which was increased by Au and Ag doping. The synthesized materials were used for the photocatalytic degradation of mixed dyes {methylene blue (MB) + methyl orange (MO) + rhodamine B (RhB)}. The observed photocatalytic degradation rate over the photocatalysts was in the order, RhB MB 蠐 MO. The photocatalytic degradation activity of the synthesized materials was observed in the order, Au-ZnS ≈ Ag-ZnS 蠐 ZnS ZnO. ZnO was ~6 times more efficient in the photocatalytic synthesis of 2-hydroxyterephthalic acid than the ZnS and metal-doped ZnS. These results further support the importance and wide applications of the synthesized ZnS, Ag-ZnS, Au-ZnS and ZnO microspheres.

Graphene nanodots decorated ultrathin P doped ZnO nanosheets as highly efficient photocatalysts

Zhu, Yuankun,Bu, Xiuming,Wang, Ding,Wang, Ping,Chen, Aiying,Li, Qian,Yang, Junhe,Wang, Xianying

, p. 78846 - 78851 (2016)

A novel kind of highly efficient photocatalyst composed of ultrathin P doped ZnO (ZnO:P) nanosheets decorated with graphene nanodots (GNDs) was fabricated. Taking the unique advantages of the ultrathin ZnO nanosheet structure, and the excellent properties

Enhanced oxidase/peroxidase-like activities of aptamer conjugated MoS2/PtCu nanocomposites and their biosensing application

Qi, Cui,Cai, Shuangfei,Wang, Xinhuan,Li, Jingying,Lian, Zheng,Sun, Shanshan,Yang, Rong,Wang, Chen

, p. 54949 - 54955 (2016)

Hybrid composite materials are particularly useful and offer great opportunities for catalysis due to their multifunctionalities. Taking advantage of the high catalytic properties of bimetallic alloy nanoparticles, the large specific surface area and co-catalytic function of MoS2 nanosheets, we prepare a novel MoS2/PtCu nanocomposite with intrinsic high oxidase- and peroxidase-like activity. The preparation of MoS2/PtCu nanocomposites does not require organic solvents or high temperature. The introduction of single-layer MoS2 nanosheets not only improves porous PtCu nanoparticles with a fine dispersion, but also readily incorporates recognition elements. As a mimic oxidase, the independence of hydrogen peroxide shows the good biocompatibility of MoS2/PtCu for promising bioapplications. On the basis of oxidase-like activity, a novel colorimetric aptasensor (apt-MoS2/PtCu) was developed and its application in the colorimetric detection of cancer cells with different MUC1-protein densities was demonstrated. The as-prepared apt-MoS2/PtCu shows good sensitivity and selectivity to targeting cells. The proposed strategy will facilitate the utilization of MoS2-based nanocomposites with high oxidase/peroxidase activities in biotechnology, biocatalysis etc.

Ionic-Liquid-Assisted Microwave Synthesis of Solid Solutions of Sr1?xBaxSnO3 Perovskite for Photocatalytic Applications

Alammar, Tarek,Slowing, Igor I.,Anderegg, Jim,Mudring, Anja-Verena

, p. 3387 - 3401 (2017)

Nanocrystalline Sr1?xBaxSnO3 (x=0, 0.2, 0.4, 0.8, 1) perovskite photocatalysts were prepared by microwave synthesis in an ionic liquid (IL) and subsequent heat-treatment. The influence of the Sr/Ba substitution on the stru

Enhancing gas adsorption and separation capacity through ligand functionalization of microporous metal-organic framework structures

Zhao, Yonggang,Wu, Haohan,Emge, Thomas J.,Gong, Qihan,Nijem, Nour,Chabal, Yves J.,Kong, Lingzhu,Langreth, David C.,Liu, Hui,Zeng, Heping,Li, Jing

, p. 5101 - 5109 (2011)

Hydroxyl- and amino- functionalized [Zn(BDC)(TED)0.5] ·2DMF·0.2H2O leads to two new structures, [Zn(BDC-OH)(TED)0.5]·1.5DMF·0.3H2O and [Zn(BDC-NH2)(TED)0.5]·xDMF·yH2O (BDC=terephthalic acid, TED=triethylenediamine, BDC-OH=2-hydroxylterephthalic acid, BDC-NH2=2-aminoterephthalic acid). Single-crystal X-ray diffraction and powder X-ray diffraction studies confirmed that the structures of both functionalized compounds are very similar to that of their parent structure. Compound [Zn(BDC)(TED)0.5]·2DMF·0.2H 2O can be considered a 3D porous structure with three interlacing 1D channels, whereas both [Zn(BDC-OH)(TED)0.5]·1.5DMF·0. 3H2O and [Zn(BDC-NH2)(TED)0.5] ·xDMF·yH2O contain only 1D open channels as a result of functionalization of the BDC ligand by the OH and NH2 groups. A notable decrease in surface area and pore size is thus observed in both compounds. Consequently, [Zn(BDC)(TED)0.5]·2DMF·0. 2H2O takes up the highest amount of H2 at low temperatures. Interestingly, however, both [Zn (BDC-OH)(TED)0.5] ·1.5DMF·0.3H2O and [Zn(BDC-NH2)(TED) 0.5] ·xDMF·yH2O show significant enhancement in CO2 uptake at room temperature, suggesting that the strong interactions between CO2 and the functionalized ligands, indicating that surface chemistry, rather than porosity, plays a more important role in CO2 adsorption. A comparison of single-component CO2, CH4, CO, N2, and O2 adsorption isotherms demonstrates that the adsorption selectivity of CO2 over other small gases is considerably enhanced through functionalization of the frameworks. Infrared absorption spectroscopic measurements and theoretical calculations are also carried out to assess the effect of functional groups on CO2 and H2 adsorption potentials.

Preparation of a ZnO/TiO2 vertical-nanoneedle-on-film heterojunction and its photocatalytic properties

Li, Delong,Zhang, Yupeng,Wu, Wenhui,Pan, Chunxu

, p. 18186 - 18192 (2014)

This paper introduces a process to prepare a novel ZnO/TiO2 heterojunction composite with ZnO nanoneedles vertically grown on a TiO 2 film via micro-arc oxidation (MAO), pulse plating and thermal oxidation. Firstly a TiO2

Magnetite/bi-doped carboxylate-rich carbon spheres-a highly efficient magnetic photocatalyst based on dimetallic FeII/FeIII and BiIII/BiIV photoredox cycles

Luo, Zhijun,Qu, Lingling,Han, Tingting,Zhang, Zhen,Shao, Xiaoling,Wu, Xiangyang,Chen, Zhong-Lin

, p. 994 - 1000 (2014)

A new magnetically separable visible-light photocatalyst, magnetite/Bi-doped carboxylate-rich carbon spheres (Bi-MCRCSs), was synthesized under ultrasonic irradiation by using magnetite/carboxylate-rich carbon spheres (MCRCSs) as a precursor. The Bi-MCRCS

Ti0.89Si0.11O2 single crystals bound by high-index {201} facets showing enhanced visible-light photocatalytic hydrogen evolution

Wu, Long,Jiang, Hai Bo,Tian, Feng,Chen, Zhigang,Sun, Chenghua,Yang, Hua Gui

, p. 2016 - 2018 (2013)

Silicon (Si) doped anatase titanium dioxide (Ti0.89Si 0.11O2) single crystals bound by high-index {201} facets and high-energy {001} facets were synthesized by a facile method. It was found that the Si-doping can widely ex

Cu(0) nanoparticle-decorated functionalized reduced graphene oxide sheets as artificial peroxidase enzymes: Application for colorimetric detection of Cr(vi) ions

Borthakur, Priyakshree,Boruah, Purna K.,Das, Manash R.,Szunerits, Sabine,Boukherroub, Rabah

, p. 1404 - 1414 (2019)

Graphene oxide (GO) sheets were functionalized by a "click" chemistry approach using azide modified GO and alkynyl-terminated d(+)-glucose precursors to produce glucose terminated hydrophilic GO surfaces. This hydrophilic functionalized GO surface was uti

Mechanistic study of visible light driven photocatalytic degradation of EDC 17α-ethinyl estradiol and azo dye Acid Black-52: Phytotoxicity assessment of intermediates

Naraginti, Saraschandra,Li, Yi,Wu, Yunbo,Zhang, Chi,Upreti, Akhanda Raj

, p. 87246 - 87257 (2016)

The present study evaluated the phytotoxicity of degraded intermediates of an endocrine-disrupting compound (EDC) 17α-ethinyl estradiol (EE2) and toxic azo dye Acid Black-52 (AB-52) in photocatalytic degradation. A novel bimetallic (silver and zirconium)

Terephthalic acid: A dosimeter for the detection of hydroxyl radicals in vitro

Barreto, Jose C.,Smith, Gregory S.,Strobel, Nathaniel H. P.,McQuillin, Pamela A.,Miller, Thomas A.

, p. PL89-PL96 (1994)

Hydroxylation reactions of aromatic compounds have been used to detect hydroxyl radicals produced by gamma irradiation and ultrasound. The present study investigated the suitability of terephthalic acid (THA) as a hydroxyl radical dosimeter for general us

Sonocatalytic performance of AgBr in the degradation of organic dyes in aqueous solution

Wu, Yun,Song, Limin,Zhang, Shujuan,Wu, Xiaoqing,Zhang, Shuna,Tian, Haifeng,Ye, Jiayi

, p. 14 - 18 (2013)

AgBr sonocatalysts were prepared by a simple method. The AgBr sonocatalysts exhibited excellent sonocatalytic activities against the decolorization of methylene blue, rhodamine B, and methyl orange. By determining the content of ·OH radicals in the ultras

One-step hydrothermal synthesis of C, W-codoped mesoporous TiO2 with enhanced visible light photocatalytic activity

Xiao, Qi,Gao, Lan

, p. 286 - 292 (2013)

C, W-codoped mesoporous TiO2 is prepared by one-step hydrothermal method and characterized by X-ray diffraction (XRD), Raman spectra, transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoe

Visible-light-responsive β-Rhombohedral boron photocatalysts

Liu, Gang,Yin, Li-Chang,Niu, Ping,Jiao, Wei,Cheng, Hui-Ming

, p. 6242 - 6245 (2013)

It's elemental! β-Rhombohedral boron was investigated as an elemental photocatalyst. Boron crystals were found to be photocatalytically active in the generation of .OH radicals under irradiation with visible light (see picture); however, the pr

Microwave-induced catalytic oxidation of malachite green under magnetic Cu-ferrites: New insight into the degradation mechanism and pathway

Liu, Xueyan,An, Shuai,Shi, Wen,Yang, Qi,Zhang, Lei

, p. 243 - 250 (2014)

Increasing attention has been paid to magnetic ferrites due to their high catalytic activity toward environmental contaminants. However, there is little information related to the generation of active species by magnetic ferrites under microwave (MW) irra

The influence of the morphology of 1D TiO2 nanostructures on photogeneration of reactive oxygen species and enhanced photocatalytic activity

Rosales, Maibelin,Zoltan, Tamara,Yadarola, Ciro,Mosquera, Edgar,Gracia, Francisco,García, Andreina

, p. 59 - 69 (2019)

The influence of morphology in one-dimensional (1D) TiO2 nanostructures—specifically nanotubes (TNT), nanofibers (TNF), nanorods (TNR), and nanowires (TNW)—on the photogeneration of reactive oxygen species (ROS) and the resulting effect on phot

Modification of tungsten trioxide with ionic liquid for enhanced photocatalytic performance

Liu, Jingjing,Han, Suiqi,Li, Jia,Lin, Jun

, p. 37556 - 37562 (2014)

To develop WO3, a narrow band gap semiconductor with a deep valence band, into an efficient visible light photocatalyst, we modified WO 3 with an ionic liquid [Bmim]I through a facile impregnation method in this study. Upon visible l

Fluorogenic naked eye “turn-on” sensing of hypochlorous acid by a Zr-based metal organic framework

Biswas, Shyam,Ghosh, Subhrajyoti,Nandi, Soutick,S. K., Mostakim

supporting information, p. 14211 - 14217 (2021/08/16)

Hypochlorous acid (HOCl) is involved in several physiological and pathological functions. Hence, sensitive and accurate detection of HOCl is much needed. We report herein a new (dimethylthiocarbamoyl)oxy functionalized aqua stable Zr-UiO-66 MOF for the specific fluorogenic recognition of HOCl in a pure aqueous medium. The activated material (1′) exhibited a dramatic increase in emission intensity (~46-fold) in the presence of HOCl. More importantly, the material has remarkable selectivity towards HOCl over other reactive oxygen species (ROS) and reactive nitrogen species (RNS). The “turn-on” nature of the material after the inclusion of HOCl could be detected by the naked eye under a UV lamp. Furthermore, a linear steady increase was observed with the gradual addition of HOCl solution over a wide linear range of 0-28 μM and the estimated LOD value was found to be 1.22 μM. HOCl-mediated oxidative cleavage of the pendant from the (dimethylthiocarbamoyl)oxy functionality to the hydroxyl functionality is the main reason behind the dramatic fluorescence enhancement of the present compound. The present compound is the first ever MOF based detector for the “turn-on” sensing of HOCl.

DIMER COMPOUNDS, AND USE IN BINDING TOXIC REPEATS OF RNA

-

Paragraph 0131; 0132, (2020/07/16)

Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are dimeric inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.

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