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2938-49-0

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2938-49-0 Usage

General Description

2,2-dimethyl-5-oxo-5-phenylpentanoic acid is a chemical compound with the molecular formula C13H16O3. It is also known by its systematic name, 2,2-dimethyl-5-oxo-5-phenylpentanoic acid. 2,2-dimethyl-5-oxo-5-phenylpentanoic acid belongs to the class of organic compounds known as fatty acids and conjugates. It is a derivative of valproic acid and is used as an anticonvulsant medication in the treatment of epilepsy and bipolar disorder. Its chemical structure consists of a five-carbon chain with a phenyl group as a substituent and a ketone group. 2,2-dimethyl-5-oxo-5-phenylpentanoic acid has potential therapeutic applications and is used in pharmaceutical formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 2938-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2938-49:
(6*2)+(5*9)+(4*3)+(3*8)+(2*4)+(1*9)=110
110 % 10 = 0
So 2938-49-0 is a valid CAS Registry Number.

2938-49-0SDS

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 2,2-dimethyl-5-oxo-5-phenylpentanoic acid

1.2 Other means of identification

Product number -
Other names 4-Benzoyl-2,2-dimethyl-buttersaeure

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:2938-49-0 SDS

2938-49-0Relevant articles and documents

Cyanohydrin-Mediated Cyanation of Remote Unactivated C(sp3)-H Bonds

Wang, Min,Huan, Leitao,Zhu, Chen

, p. 821 - 825 (2019/01/26)

A new approach for generation of alkoxy radical from the O-H bond of cyanohydrin promoted by visible-light photoredox catalysis is reported. The alkoxy radical triggers the successive remote HAT and intramolecular cyano migration, leading to the regiosele

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