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109241-76-1

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109241-76-1 Usage

Structure

A hexanoic acid derivative with a hydroxy group and a thiophene ring attached to the phenyl group.

Type

A synthetic derivative of natural compounds known as phenolic lipids.

Therapeutic properties

Antioxidant, anti-inflammatory, and neuroprotective effects.

Uses

Research and pharmaceutical development for potential medicinal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 109241-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,4 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109241-76:
(8*1)+(7*0)+(6*9)+(5*2)+(4*4)+(3*1)+(2*7)+(1*6)=111
111 % 10 = 1
So 109241-76-1 is a valid CAS Registry Number.

109241-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-hydroxy-5-(thiophene-2-carbonyl)phenyl]hexanoic acid

1.2 Other means of identification

Product number -
Other names -

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:109241-76-1 SDS

109241-76-1Downstream Products

109241-76-1Relevant articles and documents

5-Acyl-3-substituted-benzofuran-2(3H)-ones as potential antiinflammatory agents

Chakrabarti,Eggleton,Gallagher,Harvey,Hicks,Kitchen,Smith

, p. 1663 - 1668 (2007/10/02)

A series of 5-acyl-3-substituted-benzofuran-2(3H)-ones and their respective ring-opened o-hydroxy acids were synthesized. The antiinflammatory activity was evaluated in terms of their ability to improve adjuvant induced arthritis in rats. Their effect on

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