94-76-8 Usage
Description
[(4-chloro-2-methylphenyl)thio]acetic acid, also known as 4-chloro-2-methylthiophenyl acetic acid, is a chemical compound with the molecular formula C9H9ClOS. It is a thioether derivative of acetic acid and belongs to the class of aromatic acetic acids. [(4-chloro-2-methylphenyl)thio]acetic acid is recognized for its unique structural features and reactivity, making it a valuable building block in organic synthesis. Its potential applications extend beyond synthesis, as it has also been studied for its possible roles as a ligand for metal catalysts and a precursor in the production of various functionalized organic molecules. Furthermore, research has explored its potential biological activities and therapeutic properties.
Uses
Used in Pharmaceutical Synthesis:
[(4-chloro-2-methylphenyl)thio]acetic acid is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure and reactivity allow for the creation of a wide range of medicinal compounds with different therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, [(4-chloro-2-methylphenyl)thio]acetic acid serves as a crucial building block for the development of new agrochemicals. Its incorporation into these products can enhance their effectiveness in protecting crops and improving overall agricultural productivity.
Used as a Ligand for Metal Catalysts:
[(4-chloro-2-methylphenyl)thio]acetic acid is utilized as a ligand for metal catalysts in the chemical industry. Its properties enable it to improve the efficiency and selectivity of catalytic reactions, leading to more sustainable and cost-effective production processes.
Used as a Precursor in Organic Synthesis:
[(4-chloro-2-methylphenyl)thio]acetic acid is also used as a precursor in the production of various functionalized organic molecules. Its unique structural features make it an attractive starting material for the synthesis of complex organic compounds with potential applications in materials science, pharmaceuticals, and other industries.
Used in Research and Development:
[(4-chloro-2-methylphenyl)thio]acetic acid is employed in research and development for exploring its potential biological activities and therapeutic properties. Its unique structure and reactivity make it a promising candidate for the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 94-76-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94-76:
(4*9)+(3*4)+(2*7)+(1*6)=68
68 % 10 = 8
So 94-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO2S/c1-6-4-7(10)2-3-8(6)13-5-9(11)12/h2-4H,5H2,1H3,(H,11,12)
94-76-8Relevant articles and documents
Selenium analogs of phenoxypropionic and phenoxyacetic herbicides
Zakrzewski, Jerzy,Huras, Bogumi?a,Kie?czewska, Anna,Krawczyk, Maria
, p. 1005 - 1013 (2018/11/23)
Selenium analogs of phenoxyacetic herbicides, namely 2-(2,4-dichlorophenoxy)propionic acid (2,4-DP), 2-(2,4-dichlorophenoxy)acetic acid (2,4-D), 2-(4-chloro-2-methylphenoxy)propionic acid (MCPP), 2-(4-chloro-2-methylphenoxy)acetic acid (MCPA), 2-(2,4,5-trichlorophenoxy)propionic acid (2,4,5-TP), and 2-(2,4,5-trichlorophenoxy)acetic acid (2,4,5-T), were synthesized in two steps. Iodo aryl derivatives were dimerized with elemental selenium in the presence of CuO as catalyst to the corresponding diselenides. Diselenides were reduced with NaBH4 to a selenide anion and condensed with either propionic or chloroacetic acid to achieve the selenium analogs of phenoxyacetic herbicides. These selenium analogs show moderate herbicidal and fungistatic activity.
