Welcome to LookChem.com Sign In|Join Free
  • or
2-Hydroxyterephthalic acid, also known as 2-HTA, is an organic compound with the molecular formula C8H6O4. It is a white crystalline solid that is widely used in various industries due to its unique properties. 2-hydroxyterephthalic acid features a hydroxyl group and a carboxyl group attached to a terephthalic acid backbone, which allows for versatile chemical reactions and applications.

636-94-2

Post Buying Request

636-94-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

636-94-2 Usage

Uses

Used in Nanotechnology:
2-Hydroxyterephthalic acid is used as a reagent and reactant in the field of nanotechnology for its ability to interact with and manipulate nanoscale materials. It plays a crucial role in the development of advanced nanostructures and materials with improved properties.
Used in Material Science:
In the field of material science, 2-hydroxyterephthalic acid is utilized as a building block for the synthesis of various polymers and composites. Its unique chemical structure allows for the creation of materials with enhanced properties, such as improved mechanical strength, thermal stability, and energy efficiency.
Used in Energy Efficiency:
2-Hydroxyterephthalic acid has been enhanced for energy efficiency, making it a valuable component in the development of energy-saving materials and technologies. Its incorporation into materials can lead to improved insulation, reduced energy consumption, and overall increased energy efficiency in various applications.

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

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • 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 academic research and scientific papers

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.

A visible-light-driven solid state photo-Fenton reagent based on magnetite/carboxylate-rich carbon spheres

Luo, Zhijun,Tang, Hongjun,Qu, Lingling,Han, Tingting,Wu, Xiangyang

, p. 5710 - 5713 (2012)

A visible-light-driven solid state photo-Fenton reagent based on magnetite/carboxylate-rich carbon spheres (MCRCSs) has been one-step fabricated via hydrothermal carbonization (HTC) process. Without using H2O 2, MCRCSs exhibit excell

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

Synthesis of ZnO Nanoparticles Assisted by N Sources and their Application in the Photodegradation of Organic Contaminants

da Silva, Gelson T. S. T.,Carvalho, Kele T. G.,Lopes, Osmando F.,Gomes, Eliziana S.,Malagutti, Andréa R.,Mastelaro, Valmor R.,Ribeiro, Caue,Mour?o, Henrique A. J. L.

, p. 3795 - 3804 (2017)

A modified polymeric precursor method assisted by N sources (urea or melamine) was used to obtain anion-doped ZnO nanoparticles. The influence of these molecules on the physical-chemical and photocatalytic properties of the as-synthesized samples was inve

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

Microwave-Assisted Synthesis of Perovskite SrSnO3 Nanocrystals in Ionic Liquids for Photocatalytic Applications

Alammar, Tarek,Hamm, Ines,Grasmik, Viktoria,Wark, Michael,Mudring, Anja-Verena

, p. 6920 - 6932 (2017)

Nanosized SrSnO3 photocatalysts have been successfully synthesized by microwave synthesis in various ionic liquids (ILs) followed by a heat treatment process to optimize the materials' crystallinity. The influence of the ILs with various cation

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

Correlations between photocatalytic activity and chemical structure of Cu-modified TiO2–SiO2 nanoparticle composites

?i?mar,?tangar, U. Lavren?i?,Ar?on

, p. 155 - 160 (2017)

Copper-modified TiO2–SiO2 photocatalysts were prepared by sol–gel method based on organic copper, silicon and titanium precursors. Copper concentration varied from 0.1 to 3.0?mol%. A widely applied model reaction of photocatalytic ox

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

Magnetic nano-sized cadmium ferrite as an efficient catalyst for the degradation of Congo red in the presence of microwave irradiation

Shi, Wen,Liu, Xueyan,Zhang, Tingting,Wang, Qiong,Zhang, Lei

, p. 51027 - 51034 (2015)

A highly active nano-sized CdFe2O4 catalyst was prepared by a hydrothermal process and characterized by X-ray diffraction (XRD), scanning electronic microscopy (SEM), BET specific surface area method, and vibrating sample magnetometer (VSM) at room temperature. Application of the microwave-induced catalytic degradation method in the abatement of Congo red (CR) using the magnetic catalyst was studied. The degradation ratio of CR with CdFe2O4 reached 94.4% with 10 min microwave irradiation (MW), proving CdFe2O4 to be an excellent microwave catalyst. The intermediate products from CR degradation were investigated by UV-Vis, HPLC and ion chromatography. The reaction kinetics, effects of different ion species (SO42-, NO3-, HCO3-, and CH3COO-), pH of the solution, dye initial concentration, dosage of catalyst, as well as degradation mechanism were comprehensively studied. Radical trapping studies and the fluorescence technique revealed the holes (h+) and hydroxyl radicals (OH) were involved as the main active species in the reaction. The band structure of CdFe2O4 was analyzed by UV-Vis diffuse reflectance spectroscopy and Mott-Schottky measurements. The mechanism of the degradation was discussed in detail. This work can provide an effective technology for dye wastewater treatment.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 636-94-2