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2-[(2,6-Dichloropyridin-4-yl)thio]acetic acid is a chemical compound that belongs to the class of organohalogen compounds, specifically a heteroaryl halide. It is characterized by the presence of two chlorine atoms, as indicated by the prefix "di," and a pyridine ring, a basic heterocyclic organic compound. The term "thio" in its name signifies the inclusion of a sulphur atom, while "acetic acid" points to the presence of a carboxylic acid group. The molecular structure of 2-[(2,6-DICHLOROPYRIDIN-4-YL)THIO]ACETIC ACID is composed of various functional groups, which may endow it with a wide array of potential properties and applications, such as in pharmaceuticals, agrochemicals, and materials science. Further research or analysis of related chemicals would be necessary to determine its specific characteristics, uses, and potential effects on human health or the environment.

80542-50-3

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80542-50-3 Usage

Uses

Used in Pharmaceutical Industry:
2-[(2,6-Dichloropyridin-4-yl)thio]acetic acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique molecular structure, which includes a pyridine ring and a carboxylic acid group, may contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2-[(2,6-Dichloropyridin-4-yl)thio]acetic acid is used as a building block in the creation of agrochemicals, such as pesticides and herbicides. Its chemical properties, including the presence of chlorine atoms and a sulphur atom, may enhance the effectiveness of these products in controlling pests and weeds in agricultural settings.
Used in Materials Science:
2-[(2,6-Dichloropyridin-4-yl)thio]acetic acid is used as a component in the development of new materials with specific properties. Its diverse functional groups may allow for the creation of materials with unique characteristics, such as improved stability, reactivity, or other desirable traits, for use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 80542-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,4 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80542-50:
(7*8)+(6*0)+(5*5)+(4*4)+(3*2)+(2*5)+(1*0)=113
113 % 10 = 3
So 80542-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl2NO2S/c8-5-1-4(2-6(9)10-5)13-3-7(11)12/h1-2H,3H2,(H,11,12)

80542-50-3SDS

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-(2,6-dichloropyridin-4-yl)sulfanylacetic acid

1.2 Other means of identification

Product number -
Other names 2-[(2,6-Dichloropyridin-4-yl)thio]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:80542-50-3 SDS

80542-50-3Relevant academic research and scientific papers

Synthesis and anti-MRSA activity of novel cephalosporin derivatives

D'Andrea, Stan V.,Bonner, Daniel,Bronson, Joanne J.,Clark, Junius,Denbleyker, Ken,Fung-Tomc, Joan,Hoeft, Shelley E.,Hudyma, Thomas W.,Matiskella, John D.,Miller, Raymond F.,Misco, Peter F.,Pucci, Michael,Sterzycki, Roman,Tsai, Yuan,Ueda, Yasutsuga,Wichtowski, John A.,Singh, Janak,Kissick, Thomas P.,North, Jeffery T.,Pullockaran, Annie,Humora, Michael,Boyhan, Brenda,Vu, Truc,Fritz, Alan,Heikes,Fox, Rita,Godfrey, Jollie D.,Perrone, Robert,Kaplan, Murray,Kronenthal, David,Mueller, Richard H.

, p. 5687 - 5698 (2000)

Cephalosporin derivatives containing a unique combination of lipophilic C-7 sidechains and polar C-3 thiopyridinium groups were synthesized and found to exhibit potent anti-MRSA activity in vitro and in vivo. The optimum C-7 sidechains utilized were 2,5-dichlorophenylthioacetamido and 2,6-dichloropyrid-4-ylthioacetamido. The C-3 thiopyridinium rings were substituted at nitrogen with amino acid and pyruvic acid groups that were designed to confer aqueous solubility as required for IV formulation. This paper describes the characteristics of these novel cephalosporins and highlights synthetic methods developed to allow their practical, large-scale syntheses. (C) 2000 Elsevier Science Ltd.

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