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2-(5-CHLORO-3-METHYLBENZO[B]THIOPHEN-2-YL)ACETIC ACID is a chemical compound with a molecular formula C12H9ClO2S. It is a carboxylic acid that features a benzo[b]thiophene core with a 5-chloro-3-methyl substituent and an acetic acid moiety. 2-(5-CHLORO-3-METHYLBENZO[B]THIOPHEN-2-YL)ACETIC ACID belongs to the family of benzoic acids and derivatives, and is known for its anti-inflammatory and analgesic properties, making it a valuable entity in the pharmaceutical industry.

51527-19-6

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51527-19-6 Usage

Uses

Used in Pharmaceutical Industry:
2-(5-CHLORO-3-METHYLBENZO[B]THIOPHEN-2-YL)ACETIC ACID is used as an active pharmaceutical ingredient for its anti-inflammatory and analgesic properties, serving as a potential treatment for pain and inflammation.
Used as a Chemical Intermediate:
In the chemical synthesis process, 2-(5-CHLORO-3-METHYLBENZO[B]THIOPHEN-2-YL)ACETIC ACID is used as a chemical intermediate for the production of various pharmaceutical compounds, contributing to the development of new medications with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 51527-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,2 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51527-19:
(7*5)+(6*1)+(5*5)+(4*2)+(3*7)+(2*1)+(1*9)=106
106 % 10 = 6
So 51527-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9ClO2S/c1-6-8-4-7(12)2-3-9(8)15-10(6)5-11(13)14/h2-4H,5H2,1H3,(H,13,14)

51527-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-Chloro-3-methylbenzo[b]thiophen-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-(5-chloro-3-methyl-1-benzothiophen-2-yl)acetic 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:51527-19-6 SDS

51527-19-6Upstream product

51527-19-6Downstream Products

51527-19-6Relevant academic research and scientific papers

Esters and amides containing the 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetyl moiety

-

, (2008/06/13)

Compounds of the formula STR1 wherein each X, which may be identical or different from the other X, is oxygen or imino; R1 is hydrogen, fluorine, chlorine or bromine; R2 and R3, which may be identical or different from each other, are each hydrogen; unsubstituted or mono-substituted alkyl of 1 to 6 carbon atoms, where the substituent is phenyl or dialkylamino with 1 to 3 carbon atoms in each alkyl moiety; pyridyl; or cycloalkyl of 5 to 7 carbon atoms; R2 and R3, together with each other and the nitrogen atoms to which they are attached, are pyrrolidino, piperidino, hexamethyleneimino, morpholino, N-aryl-piperazino or N-(alkyl of 1 to 3 carbon atoms)-piperazino; A is cycloalkylene of 5 to 7 carbon atoms; unsubstituted or substituted alkylene of 2 to 10 carbon atoms, where the substituents are one to two alkyls of 1 to 3 carbon atoms each, one to two carbalkoxys of 2 to 4 carbon atoms each, one to two phenyls, one to four hydroxyls, one halomethyl, one hydroxymethyl, one alkanoyloxy of 1 to 18 carbon atoms, one alkanoyloxymethyl of 1 to 18 carbon atoms in the alkanoyl moiety or one STR2 where R1, R2 and R3 have the meanings previously defined; or alkylene of 2 to 10 carbon atoms interrupted by oxygen, sulfur, sulfoxide, sulfonyl, phenyl, cyclohexyl, pyridyl, piperazino or unsubstituted or substituted imino, where the substituent on the imino group is alkyl of 1 to 6 carbon atoms, phenyl or phenylalkyl of 1 to 3 carbon atoms in the alkyl moiety; B is the acyl residue of an antiphlogistic carboxylic acid; and their non-toxic, pharmacologically acceptable acid addition salts. The compounds as well as their salts are useful as anti-inflammatories.

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