51673-52-0

Basic information

• Product Name: N-chloro-N'-tosylbenzamidine
• Synonyms: N-chloro-N'-tosylbenzamidine
• CAS NO: 51673-52-0
• Molecular Weight: 308.788
• Mol File: 51673-52-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-chloro-N'-tosylbenzamidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-chloro-N'-tosylbenzamidine(51673-52-0)
• EPA Substance Registry System: N-chloro-N'-tosylbenzamidine(51673-52-0)

Safety Data

• Hazardous Substances Data: 51673-52-0(Hazardous Substances Data)

Upstream product

• 4115-16-6 p-tolylsulfonylbenzamidine 
• 98-59-9 p-toluenesulfonyl chloride 
• 1670-14-0 benzamidine monohydrochloride 
• 4115-16-6 N-[(4-methylphenyl)sulfonyl]benzenecarboximidamide 

Downstream Products

• 110-91-8 morpholine 
• 70729-31-6 2-chloro-2-phenylpropanal 
• 4115-16-6 N-[(4-methylphenyl)sulfonyl]benzenecarboximidamide 
• 113676-41-8 4-[5-Methyl-2,5-diphenyl-1-(toluene-4-sulfonyl)-4,5-dihydro-1H-imidazol-4-yl]-morpholine 
• 113676-39-4 N-(4-methyl-benzenesulfonyl)-N'-<(2-chloro-2-methyl-1-morpholino)-propyl>-benzamidine 
• 917-93-1 2-chloroisobutyraldehyde 
• 90095-48-0 C₁₄H₁₂Cl₂N₂O₂S₂ 
• 4115-16-6 p-tolylsulfonylbenzamidine 
• 110-89-4 piperidine 
• 113676-43-0 1-[5-Methyl-2,5-diphenyl-1-(toluene-4-sulfonyl)-4,5-dihydro-1H-imidazol-4-yl]-piperidine 

Relevant articles and documents

REACTION OF N-CHLORO-N'-ARYLSULFONYL- AND N'-BENZOYLBENZAMIDINES WITH SULFUR AND SULFUR DICHLORIDE

N-(N'-Arylsulfonylbenzimidoyl)dichlorosulfimides are obtained in the reaction of N-chloro-N'-arylsulfonylbenzamidines with sulfur or sulfur dichloride.N-Chloro-N'-benzoylbenzamidine reacts with sulfur dichloride in the presence of pyridine to form N-(N'-benzoylbenzimidoyl)dichlorosulfimide.Thermolysis of the latter gives 1,3,5-triphenyl-sym-triazine.When N-chloro- or N,N-dichloro-N'-benzoylbenzamidines are heated with an excess of sulfur dichloride, 2,4-diphenyl-1,3,5-thiadiazole is formed.The reaction of N-chloro-N'-benzoylbenzamidine with thionyl chloride gives N-(N'- benzoylbenzimidoyl)sulfinylamine, which decomposes with the formation of 1,3,5-triphenyl-sym-triazine when heated in inert solvents.