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587-04-2 Usage

Chemical Properties

clear colourless to light yellow liquid

Uses

3-Chlorobenzaldehyde, is used as a medicine, dye intermediates and speciality chemicals. It is mainly used to produce medicine material and intermediate, chloral alcoholate and intermediate of acid mordant azurine-6B on dyestuff.

Synthesis Reference(s)

The Journal of Organic Chemistry, 48, p. 4053, 1983 DOI: 10.1021/jo00170a036Tetrahedron Letters, 22, p. 11, 1981 DOI: 10.1016/0040-4039(81)80027-5

Purification Methods

Purify it by low temperature crystallisation from pet ether (b 40-60o) and distillation. [Beilstein 7 H 234, 7 IV 566.]

Check Digit Verification of cas no

The CAS Registry Mumber 587-04-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 587-04:
(5*5)+(4*8)+(3*7)+(2*0)+(1*4)=82
82 % 10 = 2
So 587-04-2 is a valid CAS Registry Number.

587-04-2 Well-known Company Product Price

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  • TCI America

  • (C0124)  3-Chlorobenzaldehyde  >98.0%(GC)

  • 587-04-2

  • 25g

  • 180.00CNY

  • Detail
  • TCI America

  • (C0124)  3-Chlorobenzaldehyde  >98.0%(GC)

  • 587-04-2

  • 100g

  • 380.00CNY

  • Detail
  • TCI America

  • (C0124)  3-Chlorobenzaldehyde  >98.0%(GC)

  • 587-04-2

  • 500g

  • 890.00CNY

  • Detail
  • Alfa Aesar

  • (A13254)  3-Chlorobenzaldehyde, 97%   

  • 587-04-2

  • 25g

  • 240.0CNY

  • Detail
  • Alfa Aesar

  • (A13254)  3-Chlorobenzaldehyde, 97%   

  • 587-04-2

  • 100g

  • 850.0CNY

  • Detail
  • Alfa Aesar

  • (A13254)  3-Chlorobenzaldehyde, 97%   

  • 587-04-2

  • 500g

  • 3625.0CNY

  • Detail

587-04-2SDS

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 3-Chlorobenzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde, 3-chloro-

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:587-04-2 SDS

587-04-2Synthetic route

m-chlorobenzyl alcohol

m-chlorobenzyl alcohol

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With Oxone; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium bromide In ethyl acetate at 20℃; for 24h; Reagent/catalyst; Solvent;99%
With tert.-butylnitrite; oxygen; acetic acid In toluene at 50℃; for 1h;99%
With tert.-butylhydroperoxide In toluene at 120℃; for 4h;98%
3-chlorobenzamide
618-48-4

3-chlorobenzamide

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With samarium diiodide; phosphoric acid In tetrahydrofuran for 0.000833333h; Ambient temperature;99%
m-chlorobenzylidene diacetate
2929-92-2

m-chlorobenzylidene diacetate

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With water; Sulfate; titanium(IV) oxide In benzene for 0.166667h; Deacetylation; Heating;98%
With water; silica sulfate In benzene for 0.0166667h; Heating;98%
With iron(II) sulfate In benzene for 0.5h; Heating;96%
formic acid
64-18-6

formic acid

3-iodochlorobenzene
625-99-0

3-iodochlorobenzene

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
Stage #1: formic acid; 3-iodochlorobenzene With palladium diacetate; acetic anhydride; tricyclohexylphosphine In N,N-dimethyl-formamide at 30℃; for 1h; Inert atmosphere; Green chemistry;
Stage #2: With triethylamine In N,N-dimethyl-formamide at 80℃; for 6h; Inert atmosphere; Green chemistry;
98%
With iodine; triethylamine; triphenylphosphine In toluene at 80℃; for 2h; Sealed tube;94%
With iodine; triethylamine; triphenylphosphine In toluene at 80℃; Inert atmosphere; Sealed tube;93%
With palladium diacetate; triethylamine; dicyclohexyl-carbodiimide; tricyclohexylphosphine In N,N-dimethyl-formamide at 60℃; for 10h; Inert atmosphere; Sealed tube;56%
1-chloro-3-methylbenzene
108-41-8

1-chloro-3-methylbenzene

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With laccase at 20℃; Reagent/catalyst; Green chemistry; Enzymatic reaction;97%
With dipotassium peroxodisulfate; iron(II) acetylacetonate In water; acetonitrile at 80℃; for 3h; Catalytic behavior;95%
With laccase of Pleurotus ostreatus MTCC-1801; 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt In 1,4-dioxane at 20℃; pH=4.5; Enzymatic reaction;92%
3-Chlorostyrene
2039-85-2

3-Chlorostyrene

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With 1H-imidazole; sodium periodate; MnCl-TPP-(PEO750)4 In water; acetonitrile at 80℃; for 24h;96%
With dihydrogen peroxide In water at 100℃; for 4h;90%
With dihydrogen peroxide In water; acetonitrile at 20℃; for 8h; UV-irradiation; Sealed tube; Green chemistry;85%
m-chlorobenzylamine
4152-90-3

m-chlorobenzylamine

A

3-chlorobenzamide
618-48-4

3-chlorobenzamide

B

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With water; oxygen at 140℃; under 3800.26 Torr; for 10h;A 92%
B n/a
2-(3-chlorophenyl)-1,3-oxathiolane

2-(3-chlorophenyl)-1,3-oxathiolane

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With copper(II) nitrate monohydrate at 90℃; for 0.0833333h;92%
With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate at 20℃; for 1.5h;87%
3-chlorocinnamic acid
1866-38-2

3-chlorocinnamic acid

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With aluminum oxide; potassium permanganate In dichloromethane at 20℃;91%
With sulfuric acid; quinolinium dichromate(VI) In acetic acid at 29.9℃; Rate constant; Thermodynamic data; ΔHact, ΔSact, ΔGact; var. concentration of reagents;
2-[(3-fluorophenyl)methylene]hydrazinecarboxamide

2-[(3-fluorophenyl)methylene]hydrazinecarboxamide

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With clayfen (montmorillonite K-10, Fe(NO3)3*9H2O) for 0.0333333h; microwave irradiation;90%
aluminum oxide; ammonium cerium(IV) nitrate for 0.0111111h; microwave irradiation;82%
With bis(trimethylsilyl)chromate; Montmorillonite K10 for 0.0166667h; Solid phase reaction; Cleavage; microwave irradiation;80%
m-Chlorobenzaldehyde 2,4-Dinitrophenylhydrazone
13034-95-2

m-Chlorobenzaldehyde 2,4-Dinitrophenylhydrazone

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With potassium ferrate for 0.133333h; microwave irradiation;90%
With 1,4-dichloro-1,4-diazoniabicyclo[2,2,2]octane bischloride In water at 50℃; for 0.416667h; pH=7;86%
3-chlorobenzyl acetate
21388-93-2

3-chlorobenzyl acetate

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With methanol; potassium permanganate In ethyl acetate at 25℃; for 12h;90%
1-bromomethyl-3-chlorobenzene
766-80-3

1-bromomethyl-3-chlorobenzene

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With bismuth(III) nitrate; tetrabutyl ammonium fluoride at 100℃; for 4.5h;89%
With dihydrogen peroxide In ethanol for 10h; Heating;80%
With hexamethylenetetramine In chloroform for 1h; Heating;
With potassium carbonate; dimethyl sulfoxide at 90℃; for 2h; Kornblum Aldehyd Synthesis;
m-chlorobenzylidene diacetate
2929-92-2

m-chlorobenzylidene diacetate

acetic anhydride
108-24-7

acetic anhydride

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With solid-phase supported silica chloride In methanol at 20℃; for 0.666667h;89%
3'-Chloroacetophenone
99-02-5

3'-Chloroacetophenone

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With copper(l) iodide; oxygen In dimethyl sulfoxide at 120℃; for 13h; chemoselective reaction;89%
2-(3-chlorophenyl)-1,3-dithiane
57009-71-9

2-(3-chlorophenyl)-1,3-dithiane

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With eosin y In water; acetonitrile at 20℃; for 3h; Irradiation;89%
With water In 1,4-dioxane at 100℃; for 48h; Inert atmosphere;86%
1-chloro-3-(methoxymethyl)benzene
1515-91-9

1-chloro-3-(methoxymethyl)benzene

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With hydrogen bromide; dimethyl sulfoxide at 110℃; for 14h;88%
With nitric acid In dichloromethane at 20℃; for 1h;78%
With Cu(NO3)2-SiO2 In 2,2,4-trimethylpentane for 1h; Heating; Yield given;
With titanium(IV) oxide; silver sulfate In acetonitrile at 20℃; for 2h; UV-irradiation;
3-Chlorostyrene
2039-85-2

3-Chlorostyrene

A

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

B

3'-Chloroacetophenone
99-02-5

3'-Chloroacetophenone

Conditions
ConditionsYield
With oxygen; 1-butyl-3-methylimidazolium Tetrafluoroborate; copper(l) chloride; palladium dichloride In water at 60℃; for 24h; Wacker oxidation;A n/a
B 88%
With [PdCl2(tBu-BINC)]; oxygen In N,N-dimethyl acetamide; water at 70℃; under 760.051 Torr; for 96h; Wacker oxidation;
2-(3-chlorophenyl)-1,3-dithiolane
83521-67-9

2-(3-chlorophenyl)-1,3-dithiolane

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With iodosylbenzene In dichloromethane at 20℃; for 0.5h;88%
With sodium nitrate; sulfuric acid; silica gel In dichloromethane at 20℃; for 0.25h;85%
m-chlorobenzyl alcohol
873-63-2

m-chlorobenzyl alcohol

nitrobenzene
98-95-3

nitrobenzene

A

N-(3-chlorobenzylidene)aniline
32347-04-9, 5877-57-6

N-(3-chlorobenzylidene)aniline

B

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
With α,α,α-trifluorotoluene; titanium(IV) oxide In dodecane under 750.075 Torr; for 3h; Darkness; Inert atmosphere; Irradiation;A 87.87%
B n/a
m-aminobenzaldehyde
1709-44-0

m-aminobenzaldehyde

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

Conditions
ConditionsYield
Stage #1: m-aminobenzaldehyde With potassium nitrite at 6 - 10℃; for 1h;
Stage #2: With iron phosphite; sodium carbonate; sodium bromide; sodium nitrite at 60 - 80℃; for 26h; Temperature;
86%
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

1,2-bis(3-chlorophenyl)-1,2-ethanediol
37580-83-9

1,2-bis(3-chlorophenyl)-1,2-ethanediol

Conditions
ConditionsYield
With aluminium; potassium hydroxide In methanol at 0℃; for 1h; Inert atmosphere;100%
With sodium hydroxide; aluminium In methanol; water for 0.0833333h; pinacol coupling; microwave irradiation;94%
With niobium pentachloride; zinc In 1,4-dioxane; toluene at 0℃; for 1.5h;87%
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

3-chlorobenzoate
535-80-8

3-chlorobenzoate

Conditions
ConditionsYield
With cobalt(II) 2,9,16,23-phthalocyanine tetrasulfonic acid In water; acetonitrile at 20℃; under 760.051 Torr; for 150h; UV-irradiation;100%
With sodium perborate In acetic acid for 1.5h; steam bath;95%
With dihydrogen peroxide; 7-(trifluoromethyl)-1,10-ethyleneisoalloxazinium chloride In water; acetonitrile at 85℃; for 18h;94%
2-benzoyl-1-cyano-1,2-dihydroisoquinoline
844-25-7, 55839-33-3

2-benzoyl-1-cyano-1,2-dihydroisoquinoline

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

benzoyloxy-(3-chloro-phenyl)-isoquinolin-1-yl-methane
121451-76-1

benzoyloxy-(3-chloro-phenyl)-isoquinolin-1-yl-methane

Conditions
ConditionsYield
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In acetonitrile for 0.0833333h; ultrasound sonication;100%
ethyl acetoacetate
141-97-9

ethyl acetoacetate

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

2-acetyl-3-(3-chloro-phenyl)-acrylic acid ethyl ester
15725-23-2

2-acetyl-3-(3-chloro-phenyl)-acrylic acid ethyl ester

Conditions
ConditionsYield
With piperidine; acetic acid In toluene at 20 - 120℃;100%
With piperidine; acetic acid In isopropyl alcohol at 20℃; for 24h;97%
With piperidine; acetic acid In benzene for 1h; Heating;
diethoxyphosphoryl-acetic acid ethyl ester
867-13-0

diethoxyphosphoryl-acetic acid ethyl ester

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

ethyl (E)-3-(3-chlorophenyl)prop-2-enoate
2373-88-8, 118315-76-7, 62174-98-5

ethyl (E)-3-(3-chlorophenyl)prop-2-enoate

Conditions
ConditionsYield
Stage #1: diethoxyphosphoryl-acetic acid ethyl ester With sodium hydride In tetrahydrofuran at 23℃; for 1h;
Stage #2: m-Chlorobenzaldehyde In tetrahydrofuran for 1h;
100%
With sodium hydride In N,N-dimethyl-formamide at -60℃; Horner-Wadsworth-Emmons Olefination;95%
With tetrabutyl ammonium fluoride In tetrahydrofuran at 30℃; for 4h; Glovebox;84%
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

phenylazomalonamamidine hydrochloride
6285-64-9

phenylazomalonamamidine hydrochloride

2,8-Bis-(3-chloro-phenyl)-1,7-dihydro-purin-6-one
81976-27-4

2,8-Bis-(3-chloro-phenyl)-1,7-dihydro-purin-6-one

Conditions
ConditionsYield
at 170℃; for 1h;100%
cis, trans-1,3-dimethylaminocyclohexane
2579-20-6

cis, trans-1,3-dimethylaminocyclohexane

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

C22H24Cl2N2
1217526-97-0

C22H24Cl2N2

Conditions
ConditionsYield
In methanol at 20℃; Molecular sieve;100%
In methanol at 20℃; Molecular sieve;
2,6-dichloropyridine
2402-78-0

2,6-dichloropyridine

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

(3-chloro-phenyl)-(2,6-dichloro-pyridin-3-yl)-methanol
1360114-12-0

(3-chloro-phenyl)-(2,6-dichloro-pyridin-3-yl)-methanol

Conditions
ConditionsYield
Stage #1: 2,6-dichloropyridine With n-butyllithium; diethylamine In tetrahydrofuran; hexane at -80℃; for 1.5h; Inert atmosphere;
Stage #2: m-Chlorobenzaldehyde In tetrahydrofuran; hexane at -78 - 20℃; for 16h; Inert atmosphere;
100%
N-prenyl-N-propargyltosylamide
132330-44-0

N-prenyl-N-propargyltosylamide

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

C22H24ClNO3S
1266550-08-6

C22H24ClNO3S

Conditions
ConditionsYield
Stage #1: N-prenyl-N-propargyltosylamide With ethylmagnesium bromide In tetrahydrofuran at 50℃; for 1h;
Stage #2: m-Chlorobenzaldehyde In tetrahydrofuran at 20℃; for 3h;
100%
Stage #1: N-prenyl-N-propargyltosylamide With ethylmagnesium bromide In tetrahydrofuran at 50℃; for 1h;
Stage #2: m-Chlorobenzaldehyde In tetrahydrofuran at 20℃; for 3h;
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

2,4-bis(4’-methoxyphenylamino)-6-(4’-acetylphenylamino) s-triazine

2,4-bis(4’-methoxyphenylamino)-6-(4’-acetylphenylamino) s-triazine

C32H27ClN6O3
1422249-93-1

C32H27ClN6O3

Conditions
ConditionsYield
With potassium hydroxide In N,N-dimethyl-formamide100%
1,3-diaminoguanidine hydrochloride
36062-19-8

1,3-diaminoguanidine hydrochloride

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

2,2′-bis[(3-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

2,2′-bis[(3-chlorophenyl)methylene]carbonimidic dihydrazide monohydrochloride

Conditions
ConditionsYield
In ethanol for 16h; Reflux;100%
In ethanol for 16h; Reflux;
(E)-1-{4-[(4-acetyl-2-hydroxyphenyl)diazenyl]phenyl}ethanone

(E)-1-{4-[(4-acetyl-2-hydroxyphenyl)diazenyl]phenyl}ethanone

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

(E)-3-(3-chlorophenyl)-1-{4-[(E)-{4-[(E)-3-(3-chlorophenyl)acryloyl]-2-hydroxyphenyl}diazenyl]phenyl}prop-2-en-1-one

(E)-3-(3-chlorophenyl)-1-{4-[(E)-{4-[(E)-3-(3-chlorophenyl)acryloyl]-2-hydroxyphenyl}diazenyl]phenyl}prop-2-en-1-one

Conditions
ConditionsYield
Stage #1: (E)-1-{4-[(4-acetyl-2-hydroxyphenyl)diazenyl]phenyl}ethanone; m-Chlorobenzaldehyde With sodium hydroxide In ethanol; water at 20℃; for 0.0833333h; Claisen-Schmidt Condensation;
Stage #2: In ethanol; water for 0.166667h; Claisen-Schmidt Condensation; Microwave irradiation;
100%
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

aniline
62-53-3

aniline

acetophenone
98-86-2

acetophenone

3-(N-phenylamino)-3-(3-chlorophenyl)-1-phenylacetone

3-(N-phenylamino)-3-(3-chlorophenyl)-1-phenylacetone

Conditions
ConditionsYield
With 15T-22.4TO-S15-1123 at 59.84℃; for 6h; Mannich reaction;99.8%
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

inden-1-one
83-33-0

inden-1-one

(E)-2-(4-chlorobenzylidene)-indan-1-one
5706-17-2

(E)-2-(4-chlorobenzylidene)-indan-1-one

Conditions
ConditionsYield
Stage #1: m-Chlorobenzaldehyde; inden-1-one In ethanol for 0.0833333h; Inert atmosphere;
Stage #2: With sodium hydroxide In ethanol; water for 0.5h; Inert atmosphere;
99.7%
1,3-cylohexanedione
504-02-9

1,3-cylohexanedione

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

2,2'-(3''-chlorophenyl)methylene-bis(cyclohexane-1,3-dione)

2,2'-(3''-chlorophenyl)methylene-bis(cyclohexane-1,3-dione)

Conditions
ConditionsYield
With piperidine In ethanol; water at 20℃; for 0.333333h;99.65%
With silica gel; aniline; ytterbium(III) triflate at 20℃; for 0.0333333h; neat (no solvent, solid phase);87%
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

2-(3-chloro-phenyl)-1H-benzoimidazole
22868-35-5

2-(3-chloro-phenyl)-1H-benzoimidazole

Conditions
ConditionsYield
With alumina-supported iron(III) chloride In N,N-dimethyl-formamide at 38 - 41℃; for 1.4h; Sonication;99.5%
With manganese doped CdS nanoparticles In water at 90℃; for 1.5h; chemoselective reaction;97%
With N-ethyl-pyridinium tetrafluoroborate at 50℃; for 0.333333h; Microwave irradiation; Green chemistry;97.2%
semicarbazide hydrochloride
563-41-7

semicarbazide hydrochloride

3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

2-[(3-fluorophenyl)methylene]hydrazinecarboxamide

2-[(3-fluorophenyl)methylene]hydrazinecarboxamide

Conditions
ConditionsYield
With sodium acetate In ethanol; water at 20℃;99.2%
With sodium acetate In ethanol; water for 0.0194444h; Microwave irradiation;89.1%
With acetic acid In ethanol Reflux;77%
3-Chlorobenzaldehyde
587-04-2

3-Chlorobenzaldehyde

malononitrile
109-77-3

malononitrile

2-(3-chlorobenzylidene)malononitrile
2972-73-8

2-(3-chlorobenzylidene)malononitrile

Conditions
ConditionsYield
With polystyrene-supported DABCO In methanol at 25℃; for 0.416667h; Knoevenagel Condensation; Green chemistry;99%
With 1-hexyl-3-methylimidazolium 2-hydroxybenzoate In water at 20℃; for 0.0166667h; Knoevenagel Condensation; Sonication;99.17%
With poly-N-methyl-4-vinylpyridinium hydroxide-SiO2-Al2O3 composite at 20℃; for 0.25h; Knoevenagel condensation; Neat (no solvent);98%

587-04-2Relevant articles and documents

Hydrothermal self - sacrificing growth of polymorphous MnO2 on magnetic porous - carbon (Fe3O4@Cg/MnO2): A sustainable nanostructured catalyst for activation of molecular oxygen

Bakhtiarzadeh, Zohreh,Jang, Ho Won,Karimi, Ziba,Kim, Dokyoon,Msagati, Titus A. M.,Ramakrishna, Seeram,Rostamnia, Sadegh,Rouhani, Shamila,Shokouhimehr, Mohammadreza,Varma, Rajender S.

, (2021)

Novel core-shell carbon coated-magnetic (Fe3O4@Cg) nanoparticles supported MnO2 nanosheets (with α- and β-type structure) (Fe3O4@Cg/MnO2) are synthesized through a self-sacrificing templet method. The new hybrid material was fully characterized with Fourier transformed infrared spectroscopy, energy-dispersive X-ray spectroscopy, scanning electron microscopy, X-ray diffraction analysis (XRD), N2 adsorption/desorption analysis, and transmission electron microscopy; XRD and SEM results affirmed that α- and β-MnO2 nanosheets polymorphs onto the Fe3O4@Cg. The catalytic activity of the as-prepared nanostructured catalyst Fe3O4@Cg/MnO2 has been evaluated in O2 activation for the selective oxidation of benzyl alcohol to benzaldehyde with high conversion; it stability being confirmed by the recycling of the nanostructured catalyst with no obvious loss even after six repeated runs.

-

Yamamoto et al.

, p. 1364 (1969)

-

SBA-15 Supported Silver Catalyst for the Efficient Aerobic Oxidation of Toluene Under Solvent-Free Conditions

Chen, Lei,Chen, Yanjiao,Dai, Xuan,Guo, Jiaming,Peng, Xinhua

, (2021/12/09)

The efficient SBA-15 supported silver catalysts(Ag/SBA-15) were prepared and characterized by ICP-OES, XRD, TEM, SEM, XPS and N2 adsorption–desorption techniques. The catalysts exhibited an excellent catalytic activity for the aerobic oxidation of toluene to benzaldehyde under solvent-free conditions. Conversion of toluene and selectivity of benzaldehyde were 50% and 89% respectively over catalyst with 9.1 wt% Ag loading (10Ag/SBA-15). A wide range of substrates were tolerated under the selected reaction conditions. The kinetic study shows that the oxidation of toluene over 10Ag/SBA-15 is pseudo-first-order reaction and the activation energy Ea is 45.1?kJ/mol. A plausible mechanism involving oxygen free radicals was proposed for the aerobic oxidation reaction. Compared with the traditional method, the newly designed heterogeneous catalytic system shows better economic applicability, environmental friendliness and broader application prospects. Graphical abstract: [Figure not available: see fulltext.]

One-Pot Direct Oxidation of Primary Amines to Carboxylic Acids through Tandem ortho-Naphthoquinone-Catalyzed and TBHP-Promoted Oxidation Sequence

Kim, Hun Young,Oh, Kyungsoo,Si, Tengda

supporting information, p. 18150 - 18155 (2021/12/09)

Biomimetic oxidation of primary amines to carboxylic acids has been developed where the copper-containing amine oxidase (CuAO)-like o-NQ-catalyzed aerobic oxidation was combined with the aldehyde dehydrogenase (ALDH)-like TBHP-mediated imine oxidation protocol. Notably, the current tandem oxidation strategy provides a new mechanistic insight into the imine intermediate and the seemingly simple TBHP-mediated oxidation pathways of imines. The developed metal-free amine oxidation protocol allows the use of molecular oxygen and TBHP, safe forms of oxidant that may appeal to the industrial application.

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