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4-(5-METHYL-2-THIENYL)-4-OXOBUTYRIC ACID is a chemical compound that belongs to the family of thienyl-oxobutyric acids. It is characterized by its molecular structure consisting of a thienyl group, a methyl group, and a ketone group, along with a carboxylic acid functional group. This versatile chemical is known for its potential applications in medicine and drug development due to its unique properties and biological activities.

22988-52-9

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22988-52-9 Usage

Uses

Used in Pharmaceutical Industry:
4-(5-METHYL-2-THIENYL)-4-OXOBUTYRIC ACID is used as a key intermediate in the synthesis of various drugs and pharmaceuticals. Its unique molecular structure and functional groups make it a valuable component in the development of new medications with potential therapeutic benefits.
Used in Drug Development for Neurological and Psychiatric Conditions:
4-(5-METHYL-2-THIENYL)-4-OXOBUTYRIC ACID has been studied for its potential role in the treatment of various neurological and psychiatric disorders. Its biological activities and interactions with specific receptors or enzymes may contribute to the management or treatment of these conditions, offering new avenues for therapeutic intervention.

Check Digit Verification of cas no

The CAS Registry Mumber 22988-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22988-52:
(7*2)+(6*2)+(5*9)+(4*8)+(3*8)+(2*5)+(1*2)=139
139 % 10 = 9
So 22988-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3S/c1-6-2-4-8(13-6)7(10)3-5-9(11)12/h2,4H,3,5H2,1H3,(H,11,12)

22988-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-Methyl-thiophen-2-yl)-4-oxo-butyric acid

1.2 Other means of identification

Product number -
Other names 4-(5-methylthiophen-2-yl)-4-oxobutanoic 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:22988-52-9 SDS

22988-52-9Relevant academic research and scientific papers

ARYLAMIDES AND METHODS OF USE THEREOF

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Page/Page column 94-95, (2021/06/11)

The present disclosure relates to heterocyclic compounds, pharmaceutically acceptable salts thereof, and pharmaceutical preparations thereof. Also described herein are compositions and the use of such compounds in methods of treating diseases and conditions mediated by deficient CFTR activity, in particular cystic fibrosis.

DIRECT DYES AND COMPOSITION COMPRISING THE DYES

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Page/Page column 28; 29, (2016/07/27)

The present invention relates to novel direct dyes and compositions comprising them for dyeing keratin fibers especially human hair. The novel dyes of the present invention have benzothiophene structure providing intensive and homogeneous dyeing on kerati

Peculiarities of the behavior of succinyl dichloride in Friedel-Crafts reaction with thiophenes

Smirnov,Afanas'Ev,Belen'kii

scheme or table, p. 1199 - 1207 (2011/10/13)

The reactions of thiophene, 2-methyl-, and 2-bromothiophene with succinyl dichloride in the presence of AlCl3, TiCl4, and SnCl 4 have been studied. The effect of the acylation conditions, the relative amounts and nature of the Lewis acid on the ratio and yields of the 1,4-di(2-thienyl)-1,4-diones and 4-oxo-4-(2-thienyl)butyric acids formed have been demonstrated. Under the reaction conditions, the formation of 4,4-di(2-thienyl)but-3-enoic acids (the main products in many cases) and also 4,4-di(2-thienyl)-butyrolactones was demonstrated.

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