24197-66-8 Usage
Uses
Used in Pharmaceutical Synthesis:
S-Chloroacetyl-p-mercaptotoluene is used as an intermediate in the synthesis of various pharmaceuticals for its ability to form stable thioesters with thiols, which is crucial in the development of new drug molecules.
Used in Dye Production:
In the dye industry, S-Chloroacetyl-p-mercaptotoluene is utilized as a key intermediate, contributing to the creation of diverse dyes with specific color properties.
Used in Chemical Biology:
S-Chloroacetyl-p-mercaptotoluene is employed as a biochemical tool in chemical biology for the modification of proteins and peptides, enabling researchers to study protein functions and interactions in a controlled manner.
Used in Agrochemical Production:
S-CHLOROACETYL-P-MERCAPTOTOLUENE is used as an important building block in the production of agrochemicals, playing a vital role in the development of effective and targeted agricultural products.
Used in Organic Chemistry Research:
Due to its versatile reactivity, S-Chloroacetyl-p-mercaptotoluene is a valuable chemical in the field of organic chemistry, aiding researchers in exploring new reactions and synthesizing novel organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 24197-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,9 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24197-66:
(7*2)+(6*4)+(5*1)+(4*9)+(3*7)+(2*6)+(1*6)=118
118 % 10 = 8
So 24197-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClOS/c1-7-2-4-8(5-3-7)12-9(11)6-10/h2-5H,6H2,1H3
24197-66-8Relevant academic research and scientific papers
Silica-promoted facile synthesis of thioesters and thioethers: A highly efficient, reusable and environmentally safe solid support
Basu, Basudeb,Paul, Susmita,Nanda, Ashis K.
experimental part, p. 767 - 771 (2010/09/05)
An efficient, mild and rapid procedure for the acylation and alkylation of aromatic and aliphatic thiols mediated on a silica gel surface at room temperature is described. The protocol allows the protection of thiols under neutral heterogeneous conditions without requiring any bases or Lewis acids, and the silica gel used as the promoter can be recycled for several runs without any loss of activity.
