1315257-90-9

Basic information

• Product Name: N,4-dimethyl-N-(1-phenyl-1H-indol-2-yl)benzenesulfonamide
• Synonyms: N,4-dimethyl-N-(1-phenyl-1H-indol-2-yl)benzenesulfonamide
• CAS NO: 1315257-90-9
• Molecular Weight: 376.479
• Mol File: 1315257-90-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N,4-dimethyl-N-(1-phenyl-1H-indol-2-yl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,4-dimethyl-N-(1-phenyl-1H-indol-2-yl)benzenesulfonamide(1315257-90-9)
• EPA Substance Registry System: N,4-dimethyl-N-(1-phenyl-1H-indol-2-yl)benzenesulfonamide(1315257-90-9)

Safety Data

• Hazardous Substances Data: 1315257-90-9(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 120-72-9 indole 
• 591-50-4 iodobenzene 
• 22547-51-9 1-methyl-1-(4-tolylsulfonyl)hydrazine 
• 16096-33-6 1-phenyl-1H-indole 
• 2350-10-9 N-chloro-N-methyl-4-toluene sulphonamide 

Relevant articles and documents

N -aminopyridinium salts as precursors for N-centered radicals - Direct amidation of arenes and heteroarenes

Readily prepared N-aminopyridinium salts are valuable precursors for the generation of N-centered radicals. Reduction of these salts by single electron transfer allows for clean generation of amidyl radicals. It is shown that direct radical C-H amination of heteroarenes and arenes can be achieved with N-aminopyridinium salts under mild conditions by using photoredox catalysis.