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2-Acetyl-4-chlorothiophene

CAS No.
34730-20-6
Chemical Name:
2-Acetyl-4-chlorothiophene
Synonyms
1-(4-chlorothiophen-2-yl)ethan-1-one;Avatrombopag Impurity 26;Avatroposide impurities33;4-chloro-2-acetothiophene;2-acetyl-4-chlopothiophene;2-Acetyl-4-chlorothiophene;2-Acetyl-4-chlorothiophene, 98;1-(4-chlorothien-2-yl)ethanone;Ethanone, 1-(4-chloro-2-thienyl)-;1-(4-Chlorothiophen-2-yl)ethanone
CBNumber:
CB9690448
Molecular Formula:
C6H5ClOS
Molecular Weight:
160.62
MDL Number:
MFCD00082791
MOL File:
34730-20-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:56:34

2-Acetyl-4-chlorothiophene Properties

Boiling point 263.0±25.0 °C(Predicted)
Density 1.334
storage temp. Keep in dark place,Sealed in dry,Room Temperature
Appearance Light yellow to brown Liquid
InChI InChI=1S/C6H5ClOS/c1-4(8)6-2-5(7)3-9-6/h2-3H,1H3
InChIKey FKESGQASARHBDC-UHFFFAOYSA-N
SMILES C(=O)(C1SC=C(Cl)C=1)C

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Warning
Hazard statements  H302-H312-H331
Precautionary statements  P261-P280h-P304+P340-P311a-P405-P501a
Risk Statements  36
Safety Statements  26
RIDADR  UN2810
HazardClass  6.1
HS Code  2934999090
NFPA 704
1
2 0

2-Acetyl-4-chlorothiophene price More Price(53)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FC139326 1-(4-Chlorothiophen-2-yl)ethanone 34730-20-6 0.05kg $900 2026-06-04 Buy
Biosynth FC139326 1-(4-Chlorothiophen-2-yl)ethanone 34730-20-6 0.025kg $900 2026-06-04 Buy
Biosynth FC139326 1-(4-Chlorothiophen-2-yl)ethanone 34730-20-6 0.01kg $900 2026-06-04 Buy
Biosynth FC139326 1-(4-Chlorothiophen-2-yl)ethanone 34730-20-6 0.005kg $900 2026-06-04 Buy
Biosynth FC139326 1-(4-Chlorothiophen-2-yl)ethanone 34730-20-6 0.1kg $962.5 2026-06-04 Buy
Product number Packaging Price Buy
FC139326 0.05kg $900 Buy
FC139326 0.025kg $900 Buy
FC139326 0.01kg $900 Buy
FC139326 0.005kg $900 Buy
FC139326 0.1kg $962.5 Buy

2-Acetyl-4-chlorothiophene Chemical Properties,Uses,Production

Description

2-Acetyl-4-chlorothiophene is an oxychloride that belongs to the family of thiourea derivatives. It is synthesized by reacting phosphorus oxychloride with 2,3-dichloroacetophenone in a solvent such as dioxane or acetonitrile. The final product is purified by means of vacuum distillation and recrystallization from diethyl ether, hexane, and chlorinated hydrocarbons.

Reactions

Pd(OAc)2 catalysed the direct arylation of some functionalized halothiophene derivatives allowing the synthesis in only one step of polyfunctionalized arylated thiophenes. In the presence of 2-acetyl-4-chlorothiophene and various aryl bromides, the 5-arylation products were obtained in moderate to high yields employing only 0.5 mol% catalyst. Researchers studied the coupling of 2-acetyl-4-chlorothiophene with several aryl bromides employing 0.5 mol% Pd(OAc)2 as the catalyst and KOAc as the base. These phosphine-free catalyst reaction conditions allowed the successful coupling of several aryl bromides to more simple thiophene derivatives. Using such conditions, the 5-arylated thiophenes were obtained with high isolated yields. With this procedure, the priority for the arylation of this 2,4-disubstituted thiophene is the 5-position. Moreover, no formation of by-products, such as thiophene oligomers, due to the oxidative addition of this chlorothiophene to palladium was detected during these reactions[1]. 
2-ACETYL-4-CHLOROTHIOPHENE

Synthesis

2-Acetylthiophene

88-15-3

2-ACETYL-4-CHLOROTHIOPHENE

34730-20-6

The general procedure for the synthesis of 2-acetyl-4-chlorothiophene from 2-acetylthiophene was as follows: 1-(2-thienyl)ethanone (5 g, 39.6 mmol) was dissolved in CHCl3 (50 mL) at 0 °C and AlCl3 (16 g, 0.119 mol) was added in batches. After 30 min of reaction, a solution of Cl2 in CCl4 (0.4 M) was added slowly and dropwise through the addition funnel. The reaction mixture was gradually warmed to 25 °C over 12 h and subsequently partitioned between ice water and dichloromethane. The organic layer was washed with 1N NaOH solution, dried over Na2SO4, concentrated and purified by column chromatography (silica gel, 0.5% EtOAc in hexane solution) to afford 2-acetyl-4-chlorothiophene (2.3 g, 36% yield) as a yellow oil.LC-MS (ES) m/z = 161 (M + H)+.

References

[1] Kassem Beydoun, Henri Doucet. “Palladium-catalyzed direct 5-arylation of formyl- or acetyl-halothiophene derivatives.” Journal of Organometallic Chemistry 696 9 (2011): Pages 1749-1759.

88-15-3
34730-20-6
Synthesis of 2-Acetyl-4-chlorothiophene from 2-Acetylthiophene
Global( 197)Suppliers
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Nanjing the parson's chemical technology co., LTD 025-58786926 18951781718 zbbgz2009@163.com China 298 58
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Changzhou Wanyao Biotechnology Co., Ltd. 0519-89185693 15312551983 2410037592@qq.com China 278 55

View Lastest Price from 2-Acetyl-4-chlorothiophene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-acetyl-4-chlorothiophene pictures 2026-09-03 2-acetyl-4-chlorothiophene
34730-20-6
1kg >98% by GC 50kg Zison Pharmaceutical (Shandong) Co., Ltd.
2-ACETYL-4-CHLOROTHIOPHENE  pictures 2026-08-20 2-ACETYL-4-CHLOROTHIOPHENE
34730-20-6
$1.10 1g 99.00% 100 Tons Dideu Industries Group Limited
2-ACETYL-4-CHLOROTHIOPHENE pictures 2026-03-20 2-ACETYL-4-CHLOROTHIOPHENE
34730-20-6
$10.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd

2-Acetyl-4-chlorothiophene Spectrum

1-(4-chlorothien-2-yl)ethanone 2-Acetyl-4-chlorothiophene, 98 4-chloro-2-acetothiophene 1-(4-chlorothiophen-2-yl)ethan-1-one 1-(4-Chlorothiophen-2-yl)ethanone Ethanone, 1-(4-chloro-2-thienyl)- 2-acetyl-4-chlopothiophene Avatrombopag Impurity 26 2-ACETYL-4-CHLOROTHIOPHENE ISO 9001:2015 REACH Avatroposide impurities33 1-(3,4-dichloro-6-((4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-yl)carbamoyl)pyridin-2-yl)piperidine-4-carboxylic acid 2-Acetyl-4-chlorothiophene 34730-20-6 Intermediate Sulfur compounds