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22913-26-4

22913-26-4

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22913-26-4 Usage

Chemical Properties

Colorless to yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 22913-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,1 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22913-26:
(7*2)+(6*2)+(5*9)+(4*1)+(3*3)+(2*2)+(1*6)=94
94 % 10 = 4
So 22913-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O2S/c1-8-6(7)5-2-3-9-4-5/h2-4H,1H3

22913-26-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (H61488)  Methyl thiophene-3-carboxylate, 97%   

  • 22913-26-4

  • 1g

  • 280.0CNY

  • Detail

  • Alfa Aesar

  • (H61488)  Methyl thiophene-3-carboxylate, 97%   

  • 22913-26-4

  • 5g

  • 978.0CNY

  • Detail

  • Aldrich

  • (645559)  Methyl3-thiophenecarboxylate  97%

  • 22913-26-4

  • 645559-1G

  • 348.66CNY

  • Detail

  • Aldrich

  • (645559)  Methyl3-thiophenecarboxylate  97%

  • 22913-26-4

  • 645559-5G

  • 1,341.99CNY

  • Detail

22913-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl thiophene-3-carboxylate

1.2 Other means of identification

Product number -
Other names thiophene-3-carboxylic acid methyl ester

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:22913-26-4 SDS

22913-26-4Relevant articles and documents

A New Indirect Application of Aggregative Activation: Synthesis of Esters by Cobalt-Catalyzed Carbonylation of Aryl, Heterocyclic, and Vinyl Halides under Atmospheric Pressure

Marchal, Joel,Bodiguel, Jacques,Fort, Yves,Caubere, Paul

, p. 8336 - 8340 (2007/10/02)

Sun lamp illuminated alkoxycarbonylation of aryl, heteroaryl, and vinyl halides was performed under atmospheric pressure of CO in the presence of a cobalt catalyst in situ generated from Co(OAc)2.Illunination through a Pyrex flask was sufficient to catalyze the reaction.This process avoids the use of Co2(CO)8 and excess CH3I, which were required in the earlier procedure.A SRN1 mechanism is proposed.

SYNTHESIS OF 4-CARBOXY-2-THIABICYCLOHEPTAN-6-ONES VIA 3-CARBOXY-2,3-DIHYDROTHIOPHENES: POTENTIAL β-LACTAMASE INHIBITORS

Lange, Gerald,Savard, Marc E.,Viswanatha, Thammaiah,Dmitrienko, Gary I.

, p. 1791 - 1794 (2007/10/02)

3-Carboalkoxy-2,3-dihydrothiophenes, available by Birch reduction of thiophene-3-carboxylic acid or more efficiently by deconjugation of 2,5-dihydrothiophene-3-carboxylic acid by reaction with ethyl chloroformate and triethylamine, undergo cycloaddition reactions with dichloroketene leading to 4-carboxy-7,7-dichloro-2-thiabicycloheptan-6-ones which are of interest as potential β-lactamase inhibitors.

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