941598-60-3

Basic information

• Product Name: (+/-)-N-benzyl-N'-(1-benzyl-penten-4-yl)-sulfamide
• Synonyms: (+/-)-N-benzyl-N'-(1-benzyl-penten-4-yl)-sulfamide
• CAS NO: 941598-60-3
• Molecular Weight: 344.478
• Mol File: 941598-60-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+/-)-N-benzyl-N'-(1-benzyl-penten-4-yl)-sulfamide(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-N-benzyl-N'-(1-benzyl-penten-4-yl)-sulfamide(941598-60-3)
• EPA Substance Registry System: (+/-)-N-benzyl-N'-(1-benzyl-penten-4-yl)-sulfamide(941598-60-3)

Safety Data

• Hazardous Substances Data: 941598-60-3(Hazardous Substances Data)

Upstream product

• 103-80-0 phenylacetyl chloride 
• 64020-33-3 benzyl 3-butenyl ketone 
• 5729-65-7 1-phenyl-5-hexene-2-ol 
• 56379-96-5 benzylaminosulfonyl chloride 

Relevant articles and documents

Copper(II) carboxylate promoted intramolecular diamination of terminal alkenes: Improved reaction conditions and expanded substrate scope

The copper(II) carboxylate promoted diamination reaction has been improved by the use of the organic soluble copper(II) neodecanoate [Cu(ND)2]. Cu(ND)2 allowed the less-polar solvent dichloroethane (DCE) to be used, and as a consequence, decomposition of less-reactive substrates could be avoided. High diastereoselectivity was observed in the synthesis of 2,5-disubstituted pyrrolidines. Ureas, bis(anllines), and α-amido pyrroles derived from 2-allylaniline could also participate in the diamination reaction.