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α-Chlorobenzyl 4-chlorophenyl sulfide is an organosulfur compound characterized by its chemical formula C13H10Cl2S. It is a colorless to pale yellow crystalline solid with a molecular weight of 269.19 g/mol. α-chlorobenzyl 4-chlorophenyl sulfide is formed by the linkage of an α-chlorobenzyl group (C6H5CH2Cl) and a 4-chlorophenyl group (C6H4Cl) through a sulfur atom. It is synthesized through the reaction of α-chlorotoluene with 4-chlorothiophenol in the presence of a suitable catalyst. α-Chlorobenzyl 4-chlorophenyl sulfide is primarily used as an intermediate in the production of various agrochemicals, pharmaceuticals, and other organic compounds. Due to its reactivity and potential toxicity, it is essential to handle α-chlorobenzyl 4-chlorophenyl sulfide with care and proper safety measures.

83768-35-8

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83768-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83768-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,6 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83768-35:
(7*8)+(6*3)+(5*7)+(4*6)+(3*8)+(2*3)+(1*5)=168
168 % 10 = 8
So 83768-35-8 is a valid CAS Registry Number.

83768-35-8Relevant academic research and scientific papers

Sulfonic and Phosphonic Acids Formed by Bisulfite and Phosphite Adduct Formation with Pyrimidinones

Benneche, Tore,Strande, Per,Undheim, Kjell

, p. 448 - 454 (2007/10/02)

By analogy with carbonyl compounds, ?-electron deficient 2-pyrimidinones form adducts with sodium bisulfite and phosphite esters.Both the 3,4- and 3,6-bisulfite adducts were found.The 3,4-isomer was often predominant and was obtained isomerically pure by selective precipitation from an aqueous solution.The adduct formation is reversible in aqueous solution.The adduct was also readily cleaved by trifluoroacetic acid.With tris(trimethylsilyl) phosphite, regiospecific formation of the 3,4-adduct was observed.The corresponding 3,4-dihydro-4-phosphonic acid was prepared by methanol cleavage of the silyl ester function.

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