68820-01-9

Basic information

• Product Name: 2-(phenylselanyl)-N-tosylcyclohexanamine
• Synonyms: 2-(phenylselanyl)-N-tosylcyclohexanamine
• CAS NO: 68820-01-9
• Molecular Weight: 408.423
• Mol File: 68820-01-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(phenylselanyl)-N-tosylcyclohexanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(phenylselanyl)-N-tosylcyclohexanamine(68820-01-9)
• EPA Substance Registry System: 2-(phenylselanyl)-N-tosylcyclohexanamine(68820-01-9)

Safety Data

• Hazardous Substances Data: 68820-01-9(Hazardous Substances Data)

Upstream product

• 5707-04-0 Phenylselenyl chloride 
• 70-55-3 toluene-4-sulfonamide 
• 110-83-8 cyclohexene 
• 68820-12-2 cyclohexyl-N-tosyl aziridine 
• 14971-39-2 benzeneselenolate ion 
• 1666-13-3 diphenyl diselenide 
• 127-65-1 chloroamine-T 

Downstream Products

• 58107-57-6 4-methyl-N-(2-oxo-cyclohexyl)-benzenesulfonamide 
• 80-30-8 N-cyclohexyl-p-toluenesulfonamide 

Relevant articles and documents

Regioselective ring-opening of aziridines with diselenides and disulfides using the Zn/AlCl3 system

An efficient Zn/AlCl3-promoted highly regioselective one-pot procedure has been demonstrated for the synthesis of β-amino selenides and sulfides from a variety of diselenides/disulfides and aziridines by reductive cleavage of Se-Se and S-S bond

Pyrrolidines from olefins via radical cyclization

2,4-Disubstituted N-tosylpyrrolidines were prepared from olifeins via N- tosylaziridination, benseneselenolate ring-opening and reductive radical cyclization. Azidoselenation of olefins, followed by reduction, N-tosylation, N-allylation and reductive radical cyclization, afforded 3,4-disubstituted N- tosylpyrrolidines.