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2,2-dimethyl-5-oxo-5-phenylpentanoic acid, a chemical compound with the molecular formula C13H16O3, is a derivative of valproic acid. It belongs to the class of organic compounds known as fatty acids and conjugates. 2,2-dimethyl-5-oxo-5-phenylpentanoic acid features a five-carbon chain with a phenyl group as a substituent and a ketone group, contributing to its potential therapeutic applications and use in pharmaceutical formulations.

2938-49-0

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2938-49-0 Usage

Uses

Used in Pharmaceutical Industry:
2,2-dimethyl-5-oxo-5-phenylpentanoic acid is used as an anticonvulsant medication for the treatment of epilepsy and bipolar disorder. Its chemical structure allows it to effectively manage seizure activity and stabilize mood swings, making it a valuable component in the management of these neurological conditions.
Additionally, due to its potential therapeutic applications, 2,2-dimethyl-5-oxo-5-phenylpentanoic acid is utilized in the development of pharmaceutical formulations. Its unique properties and structural features contribute to the creation of new medications that can address a range of health concerns.

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 academic research and scientific papers

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

Studies in the Cycloheptane Series. Part - XXXI: Friedel-Crafts Reaction of the Anhydride of αα-Dimethylglutaric Acid with Different Aromatic Hydrocarbons and Synthesis of 1,1-Dimethyl-3,4-benzo/substituted benzocycloheptanes and 1,1-Dimethylthienocycloheptane

Gautam, R. K.,Kannan, S.,Saharia, G. S.

, p. 378 - 379 (2007/10/02)

The anhydride of αα-dimethylglutaric acid on condensation with benzene, toluene, isomeric xylenes, chlorobenzene, anisole, tetralin, naphthalene and thiophene under F.C. conditions gives the respective αα-dimethyl-γ-aroyl-n-butyric acids which on Clemmensen reduction yield δ-aryl-n-valeric acids.These on cyclisation with PPA furnish III and IV (X=O) which on Clemmensen reduction give the respective hydrocarbons (III and IV: X=H2).

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