138710-14-2

Upstream product

• 28031-49-4 N-butyl-4-pentenylamine 
• 931-59-9 benzenesulfenyl chloride 
• 882-33-7 diphenyldisulfane 
• 176791-66-5 N-butyl-N-4-pentenyl-4-carbomethoxybenzenesulfenamide 

Relevant academic research and scientific papers

Cyclization of N-butyl-4-pentenylaminyl: Implications for the cyclization of alkenylaminyl radicals

The utility of arenesulfenamides as aminyl radical precursors has been clearly demonstrated. The cyclization of N-butyl-4-pentenylaminyl is shown to be a slow and irreversible process that is accelerated significantly by small amounts of bis(tributyltin) oxide.

Sulphenamides as synthetic precursors of aminyl radicals

Sulphenamides, readily synthesised from reaction between benzenesulphenyl derivatives and amines, undergo facile reaction with radical generating reagents such as tributyltin hydride to yield aminyl radicals.