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6315-20-4

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6315-20-4 Usage

Description

Butanedioic acid, (3-methylphenyl)methyl-, also known as 3-Methylbenzylsuccinic Acid, is a key metabolite formed during the anaerobic transformation of m-xylene by Azoarcus sp. strain T. This bacterium is a denitrifying type capable of mineralizing m-xylene via 3-methylbenzoate. Butanedioic acid, (3-methylphenyl)methylplays a significant role in the metabolic pathway of certain bacteria, contributing to the breakdown and utilization of specific hydrocarbons.

Uses

Used in Environmental Applications:
Butanedioic acid, (3-methylphenyl)methylis used as a metabolite in the anaerobic transformation process for the degradation of m-xylene. This application is crucial for the bioremediation of environments contaminated with m-xylene, a common pollutant found in industrial settings.
Used in Microbial Metabolism Studies:
In the field of microbiology, Butanedioic acid, (3-methylphenyl)methylserves as a subject of study to understand the metabolic pathways of bacteria like Azoarcus sp. strain T. This knowledge can be applied to develop biotechnological solutions for the treatment of hydrocarbon pollution and the enhancement of biodegradation processes.
Used in Denitrification Research:
Butanedioic acid, (3-methylphenyl)methylis also used in research related to denitrification, a process in which bacteria like Azoarcus sp. strain T convert nitrate to nitrogen gas under anaerobic conditions. Understanding the role of this metabolite in the process can help in developing strategies to reduce nitrate pollution in aquatic systems and improve overall environmental health.

Check Digit Verification of cas no

The CAS Registry Mumber 6315-20-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6315-20:
(6*6)+(5*3)+(4*1)+(3*5)+(2*2)+(1*0)=74
74 % 10 = 4
So 6315-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4/c1-8-3-2-4-9(5-8)6-10(12(15)16)7-11(13)14/h2-5,10H,6-7H2,1H3,(H,13,14)(H,15,16)

6315-20-4SDS

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-[(3-methylphenyl)methyl]-Butanedioic acid

1.2 Other means of identification

Product number -
Other names (m-methylbenzyl)succinic 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:6315-20-4 SDS

6315-20-4Relevant articles and documents

A practical procedure for the synthesis of esonarimod, (R,S)-2-acetylthiomethyl-4-(4-methylphenyl)-4-oxobutanoic acid, an antirheumatic agent (part 1).

Noguchi, Toshiya,Onodera, Akira,Tomisawa, Kazuyuki,Yokomori, Sadakazu

, p. 1407 - 1412 (2007/10/03)

An efficient and practical procedure for the synthesis of esonarimod, (R,S)-2-acetylthiomethyl-4-(4-methylphenyl)-4-oxobutanoic acid (1), a new antirheumatic drug, has been developed. The intermediate, 2-methylene-4-(4-methylphenyl)-4-oxobutanoic acid (2), was prepared by Friedel-Crafts acylation of toluene with itaconic anhydride (3) in the presence of aluminum trichloride and nitrobenzene in 63% yield without silica gel column purification. Compound 1 was prepared by Michael addition of 2 with thioacetic acid (4) in 74% yield. Overall, 1 was obtained in 47% yield from 3. The structures and synthetic mechanisms of by-products (five compounds) of 2 were also clarified.

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