35160-04-4

Basic information

• Product Name: 2-benzyl-5-nitrobenzo[d]isothiazol-3(2H)-one
• Synonyms: 2-benzyl-5-nitrobenzo[d]isothiazol-3(2H)-one
• CAS NO: 35160-04-4
• Molecular Weight: 286.311
• Mol File: 35160-04-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-benzyl-5-nitrobenzo[d]isothiazol-3(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-5-nitrobenzo[d]isothiazol-3(2H)-one(35160-04-4)
• EPA Substance Registry System: 2-benzyl-5-nitrobenzo[d]isothiazol-3(2H)-one(35160-04-4)

Safety Data

• Hazardous Substances Data: 35160-04-4(Hazardous Substances Data)

Upstream product

• 92030-46-1 5,5'-dinitro-2,2'-disulfanediyl-bis-benzoyl chloride 
• 100-46-9 benzylamine 
• 106991-89-3 N,N'-dibenzyl-5,5'-dinitro-2,2'-disulfanediyl-bis-benzamide 
• 83909-69-7 N-benzyl-2-chloro-5-nitrobenzamide 

Downstream Products

• 92905-96-9 2-benzyl-5-nitro-1,1-dioxo-1,2-dihydro-1λ⁶-benzo[d]isothiazol-3-one 

Relevant articles and documents

Preparation of benzisothiazolones from 2-bromobenzamides and sulfur under copper catalysis conditions

A convenient two-stage method has been developed for preparing benz[d]isothiazol-3(2H)-ones from 2-bromobenzamides and sulfur in a one-pot process under copper catalysis conditions. The method is suitable for the synthesis of N-aryl-, benzyl-, and alkyl-substituted benzisothiazolones. The yields of the benzisothiazolones depend on the nature of the starting amide and can reach 91%.

PREPARATION OF 5-NITROBENZOISOTHIAZOLONE AND ITS N-DERIVATIVES.

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