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Butanoic acid, 2-[(acetylthio)methyl]-4-(4-methylphenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124947-23-5

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124947-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124947-23-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,9,4 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124947-23:
(8*1)+(7*2)+(6*4)+(5*9)+(4*4)+(3*7)+(2*2)+(1*3)=135
135 % 10 = 5
So 124947-23-5 is a valid CAS Registry Number.

124947-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(acetylsulfanylmethyl)-4-(4-methylphenoxy)butanoic acid

1.2 Other means of identification

Product number -
Other names Butanoic acid,2-[(acetylthio)methyl]-4-(4-methylphenoxy)

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:124947-23-5 SDS

124947-23-5Downstream Products

124947-23-5Relevant academic research and scientific papers

Structure-activity studies of 3-benzoylpropionic acid derivatives suppressing adjuvant arthritis

Kawashima,Kameo,Kato,Hasegawa,Tomisawa,Hatayama,Hirono,Moriguchi

, p. 774 - 777 (2007/10/02)

3-Benzoylpropionic acid derivatives possess an immunomodulative activity and suppress adjuvant arthritis. To understand how substituents affect the biological activity, the quantitative structure-activity relationships of 30 compounds were analyzed by the adaptive least-squares method. For the suppressing activity in rats, the electronic effects and the structural feature of the substituent on benzene ring were suggested to be important. To reinforce and confirm the correlation, 4 additional compounds of phenoxybutyric acid derivatives were synthesized and tested with the rat adjuvant-induced arthritis. These compounds were found to have potent suppressing activity.

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