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2-ACETYL-4-CHLOROTHIOPHENE

Product Name
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;4-chloro-2-acetothiophene;Avatroposide impurities33;2-ACETYL-4-CHLOROTHIOPHENE;2-acetyl-4-chlopothiophene;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
Formula Weight
160.62
MOL File
34730-20-6.mol
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2-ACETYL-4-CHLOROTHIOPHENE Property

Boiling point:
263.0±25.0 °C(Predicted)
Density 
1.334
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
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
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Safety

Risk Statements 
36
Safety Statements 
26
RIDADR 
UN2810
HazardClass 
6.1
HS Code 
2934999090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H312Harmful in contact with skin

H331Toxic if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P405Store locked up.

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N-Bromosuccinimide Price

Alfa Aesar
Product number
H30384
Product name
2-Acetyl-4-chlorothiophene, 98+%
Packaging
5g
Price
$106.65
Updated
2024/03/01
Alfa Aesar
Product number
H30384
Product name
2-Acetyl-4-chlorothiophene, 98+%
Packaging
1g
Price
$35.9
Updated
2023/06/20
Alfa Aesar
Product number
H30384
Product name
2-Acetyl-4-chlorothiophene, 98+%
Packaging
25g
Price
$392.65
Updated
2024/03/01
TRC
Product number
C611233
Product name
1-(4-chlorothiophen-2-yl)ethanone
Packaging
2.5g
Price
$155
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC139326
Product name
1-(4-Chlorothiophen-2-yl)ethanone
Packaging
10g
Price
$177
Updated
2021/12/16
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2-ACETYL-4-CHLOROTHIOPHENE Chemical Properties,Usage,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]. 

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.

2-ACETYL-4-CHLOROTHIOPHENE Preparation Products And Raw materials

Raw materials

Preparation Products

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2-ACETYL-4-CHLOROTHIOPHENE Suppliers

Alfa Aesar, Thermo Fisher Scientific
Tel
--
Fax
--
Email
es@alfa.com
Country
Germany
ProdList
5123
Advantage
58
Fox-Chemicals Gmbh
Tel
--
Fax
--
Email
info@foxchemicals.com
Country
Germany
ProdList
444
Advantage
58
CHEMOS GmbH & Co. KG
Tel
--
Fax
--
Email
chemos@chemos.de
Country
Germany
ProdList
6727
Advantage
58
ABCR GmbH & CO. KG
Tel
--
Fax
--
Email
info@abcr.de
Country
Germany
ProdList
6831
Advantage
75
ACTIVATE SCIENTIFIC GmbH
Tel
--
Fax
--
Email
info@activate-scientific.com
Country
Germany
ProdList
2856
Advantage
61
ChemPur GmbH
Tel
--
Fax
--
Email
info@ChemPur.de
Country
Germany
ProdList
2737
Advantage
50
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View Lastest Price from 2-ACETYL-4-CHLOROTHIOPHENE manufacturers

Zison Pharmaceutical (Shandong) Co., Ltd.
Product
2-acetyl-4-chlorothiophene 34730-20-6
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
>98% by GC
Supply Ability
50kg
Release date
2023-01-09
Hebei Weibang Biotechnology Co., Ltd
Product
2-ACETYL-4-CHLOROTHIOPHENE 34730-20-6
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-29
Suzhou Nordica Biopharma CO.,LTD
Product
1-(4-chlorothiophen-2-yl)ethan-1-one 34730-20-6
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
2 tons
Release date
2024-11-15

34730-20-6, 2-ACETYL-4-CHLOROTHIOPHENERelated Search:


  • 2-ACETYL-4-CHLOROTHIOPHENE
  • 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
  • 34730-20-6
  • Intermediate
  • Sulfur compounds