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N-(2,4,6-trichlorophenyl) S,S-dichlorosulfimide is a chemical compound with the formula C6H2Cl5NOS. It is a derivative of sulfimide, featuring a 2,4,6-trichlorophenyl group attached to the nitrogen atom. N-(2,4,6-trichlorophenyl) S,S-dichlorosulfimide is known for its potential use as an intermediate in the synthesis of various agrochemicals and pharmaceuticals, particularly those with pesticidal properties. Due to its reactivity and the presence of multiple chlorine atoms, it is also of interest in studies related to chemical reactivity and substitution patterns. The compound's structure and properties make it a subject of research in organic chemistry, with potential applications in the development of new compounds with specific biological activities.

6615-96-9

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6615-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6615-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6615-96:
(6*6)+(5*6)+(4*1)+(3*5)+(2*9)+(1*6)=109
109 % 10 = 9
So 6615-96-9 is a valid CAS Registry Number.

6615-96-9Upstream product

6615-96-9Relevant academic research and scientific papers

Synthetic applications and spectroscopic investigations of the (NSCl)3-SO2Cl2 system

Apblett, Allen,Chivers, Tristram

, p. 650 - 654 (2007/10/02)

Solutions of (NSCl)3 in the presence of excess SO2Cl2 behave as a source of the synthetic equivalent "NSCl3" in reactions with methacrylonitrile or thioacetamide to give 4-cyanoisothiazole (78percent) or 5-methyl-1,3,2,4-dithiadiazolium chloride (63percen

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