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2975-71-5

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2975-71-5 Usage

Structure

Contains a benzofuran ring and a benzoic acid moiety

Synthesis

Produced by the reaction of benzofuran-2-carboxylic acid and 3-formyl-5-hydroxybenzoic acid

Use

Has potential therapeutic properties and is used in the pharmaceutical industry

Pharmacological properties

Displays anti-inflammatory and antioxidant activities

Potential applications

Being investigated for the treatment of various diseases

Check Digit Verification of cas no

The CAS Registry Mumber 2975-71-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2975-71:
(6*2)+(5*9)+(4*7)+(3*5)+(2*7)+(1*1)=115
115 % 10 = 5
So 2975-71-5 is a valid CAS Registry Number.

2975-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3-oxo-1H-2-benzofuran-1-yl)methyl]benzoic acid

1.2 Other means of identification

Product number -
Other names 2-phthalidylmethyl-benzoic 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:2975-71-5 SDS

2975-71-5Relevant articles and documents

Reduction of 3-(carboxyaryl)isocoumarins with sodium borohydride

Ishchenko,Voevoda,Shablykina,Turov,Khilya

, p. 1212 - 1224 (2012/08/07)

Reduction of 3-(carboxyaryl)isocoumarins with sodium borohydride proceeds with formation of corresponding 3-carboxyaryl-3,4-dihydroisocoumarins or isomeric dihydrophthalides, 3-(2-carboxybenzyl)-2-benzofuran-1(3H)-ones. Derivatives at the carboxyl group of 3-carboxyaryl-3,4-dihydroisocoumarins and 3-(2-carboxybenzyl)-2-benzofuran-1(3H)-ones have been obtained. 0009-3122/12/4710-12122012 Springer Science+Business Media, Inc.

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