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1505-52-8

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1505-52-8 Usage

General Description

3-Methylthianaphtene-2-acetic acid, also known as 3-MTAA, is a chemical compound consisting of a thianaphthene ring with a methyl substituent and a carboxylic acid group attached at the 2-position. It is a synthetic compound that has potential applications in pharmaceuticals and organic synthesis. 3-MTAA has been studied for its anti-inflammatory and analgesic properties, and its structure makes it a potential precursor for the synthesis of novel bioactive molecules. Its unique molecular structure and potential pharmacological properties make 3-MTAA an interesting and promising compound for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1505-52-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1505-52:
(6*1)+(5*5)+(4*0)+(3*5)+(2*5)+(1*2)=58
58 % 10 = 8
So 1505-52-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O2S/c1-7-8-4-2-3-5-9(8)14-10(7)6-11(12)13/h2-5H,6H2,1H3,(H,12,13)/p-1

1505-52-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A19620)  3-Methylbenzo[b]thiophene-2-acetic acid, 97%   

  • 1505-52-8

  • 0.5g

  • 1375.0CNY

  • Detail
  • Alfa Aesar

  • (A19620)  3-Methylbenzo[b]thiophene-2-acetic acid, 97%   

  • 1505-52-8

  • 2.5g

  • 4398.0CNY

  • Detail
  • Alfa Aesar

  • (A19620)  3-Methylbenzo[b]thiophene-2-acetic acid, 97%   

  • 1505-52-8

  • 10g

  • 14812.0CNY

  • Detail

1505-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methyl-1-benzothiophen-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 3-Methylbenzo[b]thiophene-2-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:1505-52-8 SDS

1505-52-8Downstream Products

1505-52-8Relevant articles and documents

-

Gaertner

, p. 2991,2993 (1952)

-

Nickel-Catalyzed Carboxylation of Benzylic C-N Bonds with CO2

Moragas, Toni,Gaydou, Morgane,Martin, Ruben

supporting information, p. 5053 - 5057 (2016/04/26)

A user-friendly Ni-catalyzed reductive carboxylation of benzylic C-N bonds with CO2 is described. This procedure outperforms state-of-the-art techniques for the carboxylation of benzyl electrophiles by avoiding commonly observed parasitic pathways, such as homodimerization or β-hydride elimination, thus leading to new knowledge in cross-electrophile reactions.

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