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50-73-7

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50-73-7 Usage

Description

2,3,5-Trichlorobenzoic acid is a light beige crystalline powder with chemical properties that make it useful in various applications. It is a type of chlorinated benzoic acid, which is known for its ability to enhance the dechlorination of certain compounds.

Uses

Used in Environmental Applications:
2,3,5-Trichlorobenzoic acid is used as a dechlorination enhancer for Aroclor 1248, a polychlorinated biphenyl (PCB) congener. Its application is crucial in the environmental industry, as it aids in the breakdown and removal of harmful PCBs from contaminated sites, thus contributing to the remediation of polluted areas and the protection of ecosystems.
Used in Chemical Synthesis:
In the chemical industry, 2,3,5-Trichlorobenzoic acid can be utilized as an intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable building block for the development of new chemicals with potential applications in pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
2,3,5-Trichlorobenzoic acid is also employed in research and development settings, where it can be used to study the effects of chlorination on benzoic acid derivatives and to investigate the mechanisms of dechlorination. This knowledge can be applied to develop more efficient and environmentally friendly methods for the degradation of persistent organic pollutants.

Check Digit Verification of cas no

The CAS Registry Mumber 50-73-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50-73:
(4*5)+(3*0)+(2*7)+(1*3)=37
37 % 10 = 7
So 50-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)/p-1

50-73-7SDS

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 2,3,5-Trichlorobenzoic acid

1.2 Other means of identification

Product number -
Other names RARECHEM AL BE 0200

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:50-73-7 SDS

50-73-7Relevant articles and documents

Atkinson,Lawler

, p. 1704,1707 (1940)

Synthesis of some novel 2,4-disubstituted thiazoles as possible antimicrobial agents

Karegoudar, Prakash,Karthikeyan, Mari Sithambaram,Prasad, Dasappa Jagadeesh,Mahalinga, Manjathuru,Holla, Bantwal Shivarama,Kumari, Nalilu Sucheta

, p. 261 - 267 (2008/09/18)

A series of novel 4-aryl/chloroalkyl-2-(2,3,5-trichlorophenyl)-1,3-thiazoles (5a-g and 7a-e) were synthesized by condensing 2,3,5-trichlorobenzenecarbothioamide with phenacyl bromide/dichloroacetone. 2,3,5-Trichlorobenzaldehyde thiosemicarbazone on treatment with phenacyl bromide afforded 4-aryl-2-(2,3,5-trichlorophenylidenehydrazino)-1,3-thiazoles (10a-g) in good yield. The newly synthesized compounds are characterized by IR, 1H NMR and mass spectral studies. These compounds were also screened for their antibacterial and antifungal activities. Preliminary results reveal that some of the synthesized compounds are showing promising antimicrobial activity.

Pharmacologically active CNS compounds

-

, (2008/06/13)

The invention provides compounds of formula (I) wherein at least one of R1, R2 and R3 is chloro and the others are selected from hydrogen and chloro; and R4 and R5 are the same or different and are each alkyl or hydrogen. The compounds may be used for the treatment or prophylaxis of a neurodegenerative of other neurological disorder of the CNS, the aetiology of which includes excessive release of the neurotransmitter glutamate.

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