71996-32-2

Basic information

• Product Name: N-(5λ⁴-dibenzo[b,d]thiophen-5-ylidene)-4-methylbenzenesulfonamide
• Synonyms: N-(5λ⁴-dibenzo[b,d]thiophen-5-ylidene)-4-methylbenzenesulfonamide
• CAS NO: 71996-32-2
• Molecular Weight: 353.466
• Mol File: 71996-32-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(5λ⁴-dibenzo[b,d]thiophen-5-ylidene)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(5λ⁴-dibenzo[b,d]thiophen-5-ylidene)-4-methylbenzenesulfonamide(71996-32-2)
• EPA Substance Registry System: N-(5λ⁴-dibenzo[b,d]thiophen-5-ylidene)-4-methylbenzenesulfonamide(71996-32-2)

Safety Data

• Hazardous Substances Data: 71996-32-2(Hazardous Substances Data)

Upstream product

• 132-65-0 dibenzothiophene 
• 70-55-3 toluene-4-sulfonamide 
• 127-65-1 chloroamine-T 
• 1013-23-6 Dibenzothiophene sulfoxide 

Downstream Products

• 92-51-3 cyclohexylcyclohexane 
• 70-55-3 toluene-4-sulfonamide 
• 1072-95-3 cyclohexylmethyl chloride 
• 132-65-0 dibenzothiophene 
• 4435-14-7 2-cyclohexylacetonitrile 
• 68-34-8 phenyl toluenesulfonamide 
• 17436-27-0 p-tolylsulfonyliminotri(phenoxy)phosophorane 
• 116905-61-4 2-butyl-N-tosylaziridine 
• 205581-06-2 S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfimide 
• 24702-26-9 S-p-Tolyl-S-methyl-N-p-tosylsulfimid 
• 13150-76-0 N-[(4-methylphenyl)sulfonyl]-S,S-diphenyl-sulfilimine 
• 24702-28-1 S-(4-chlorophenyl)-S-methyl-N-(4-tosyl)sulfilimine 
• 15436-21-2 S-Methyl-S-p-methoxyphenyl-N-p-tosylsulfylimin 
• 1058-14-6 N-p-tolylsulfonylphosphine imide 

Relevant articles and documents

Dibenzothiophenesulfilimines: A Convenient Approach to Intermolecular Rhodium-Catalysed C?H Amidation

A sulfilimine-based Group 9 transition-metal-catalysed C?H amidation procedure is reported. Dibenzothiophene-based sulfilimines were shown to constitute a class of novel amidation reagents which enable the transfer of a wide range of N-sulfonyl and N-acyl

Generation of nitrene by the photolysis of N-substituted iminodibenzothiophene

(Chemical Equation Presented) To evaluate the ability of dibenzothiophene N-substituted sulfilimines as photochemical nitrene sources, their photolyses in the presence of several trapping reagents, such as sulfides, olefins, and phosphorus compounds, were performed. In the reactions, the corresponding imino-transfer compounds, namely sulfilimines, aziridines, and iminophosphoranes, were formed in good yields, indicating dibenzothiophene N-tosyl and N-acylsulfilimines have a potent nature as nitrogen sources.

POLAROGRAPHIC STUDY OF STRUCTURE-PROPERTIES RELATIONSHIP OF p-TOSYL SULFILIMINES

A structure-reactivity relationship for a series of eight N-p-tosyl sulfilimines and five related sulfoxides is investigated by polarographic reduction of the S-N and S-O bonds respectively.Conjugation of the tricoordinated sulfur is the dominant factor t