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(2,6-Dichloro-benzylsulfanyl)-acetic acid, also known as DCSA, is a chemical compound with potential pharmaceutical applications. It belongs to the class of acetic acid derivatives and contains a benzene ring with two chlorine atoms and a sulfanyl group attached to the carbon atom. DCSA has been studied for its potential anti-inflammatory and analgesic properties, and it may also have antitumor and antibacterial effects.

65051-35-6

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65051-35-6 Usage

Uses

Used in Pharmaceutical Industry:
(2,6-Dichloro-benzylsulfanyl)-acetic acid is used as a potential therapeutic agent for its anti-inflammatory and analgesic properties. It is being studied for its potential to treat certain diseases and alleviate pain and inflammation.
Used in Oncology:
(2,6-Dichloro-benzylsulfanyl)-acetic acid is used as a potential antitumor agent. It has shown promise in preclinical studies for the treatment of certain cancers, and further research is ongoing to explore its potential therapeutic uses in this area.
Used in Antibacterial Applications:
(2,6-Dichloro-benzylsulfanyl)-acetic acid is used as a potential antibacterial agent. Its ability to inhibit bacterial growth and reduce infection makes it a candidate for further research and development in the field of infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 65051-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,5 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65051-35:
(7*6)+(6*5)+(5*0)+(4*5)+(3*1)+(2*3)+(1*5)=106
106 % 10 = 6
So 65051-35-6 is a valid CAS Registry Number.

65051-35-6SDS

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 2-[(2,6-dichlorophenyl)methylsulfanyl]acetic acid

1.2 Other means of identification

Product number -
Other names (2,6-Dichlorobenzylsulfanyl)acetic 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:65051-35-6 SDS

65051-35-6Relevant academic research and scientific papers

IL-8 RECEPTOR ANTAGONISTS

-

, (2008/06/13)

This invention relates to novel compounds of Formula (I), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8). Compounds of Formnula (I) are represented, interalia, by structure (I) wherein i

IL-8 receptor antagonists

-

, (2008/06/13)

This invention relates to novel spiro compound derivatives of benzoisothiazolyl-urea and -thiourea and compositions thereof. These compounds are useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).

Synthesis of some sulfur-containing acylferrocenes

Vuki?evi?, Rastko D.,Ili?, Danijela,Ratkovi?, Zoran,Vuki?evi?, Mirjana

, p. 625 - 631 (2007/10/03)

Acylferrocenes containing a sulfur atom within their side chain were synthesized in good yields by Friedel-Crafts acylation of ferrocene with in situ generated acyl halides from the corresponding carboxylic acids (S-protected derivatives of thioglicolic and α- and β-mercaptopropionic acids).

Phenylamidine derivatives

-

, (2008/06/13)

A compound having the general formula: STR1 wherein Ar is an aryl group (especially an α-naphthyl, β-naphthyl or phenyl group) which may be substituted by one or more C1-4 alkyl, C1-4 alkoxy, methylenedioxy halogen, CF3, NH2 or NO2 groups; A is a --CH2 --, --CHOH--, --CH2 O--, --CH2 S--, --CH2 NH--, --OCH2 --, --SCH2 --, --NH--, --NHCOCH2 --, --CH2 NHCH2 -- or --NHCH2 -- group; Y is O or NH; and B is a single bond and, when A is --CH2 --S, may be a --CH2 --, or --CH(CH3)-- group; and their acid addition salts when Y is NH and their metal salts when Y is O. The compounds and their salts have therapeutic utility in treatment of neuropsychic ailments.

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