767358-01-0

Basic information

• Product Name: (3S,4R,5S)-5-benzylamino-4-dibenzylamino-3-hydroxy-1-propylpiperidine
• Synonyms: (3S,4R,5S)-5-benzylamino-4-dibenzylamino-3-hydroxy-1-propylpiperidine
• CAS NO: 767358-01-0
• Molecular Weight: 443.632
• Mol File: 767358-01-0.mol

Chemical Properties

• CAS DataBase Reference: (3S,4R,5S)-5-benzylamino-4-dibenzylamino-3-hydroxy-1-propylpiperidine(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4R,5S)-5-benzylamino-4-dibenzylamino-3-hydroxy-1-propylpiperidine(767358-01-0)
• EPA Substance Registry System: (3S,4R,5S)-5-benzylamino-4-dibenzylamino-3-hydroxy-1-propylpiperidine(767358-01-0)

Safety Data

• Hazardous Substances Data: 767358-01-0(Hazardous Substances Data)

Upstream product

• 767357-97-1 (2S,1'R,2'R)-1-benzyl-2-[1'-(dibenzylamino)-2',3'-epoxypropyl]aziridine 
• 107-10-8 propylamine 
• 767358-00-9 (2S,1'R)-1-benzyl-2-[1'-(dibenzylamino)-2'-oxoethyl]aziridine 
• 100-46-9 benzylamine 
• 591750-70-8 (2S,1'R)-1-benzyl-2-{1'-(dibenzylamino)-2'-[(tert-butyldimethylsilanyl)oxy]ethyl}aziridine 
• 388632-20-0 (-)-(3S)-3-(dibenzylamino)-4-[(tert-butyldimethylsilanyl)oxy]-1-chlorobutan-2-one 
• 767357-99-3 (2S,1'R)-1-benzyl-2-[1'-(dibenzylamino)-2'-hydroxyethyl]aziridine 

Relevant articles and documents

Synthesis of chiral amino epoxyaziridines: Useful intermediates for the preparation of chiral trisubstituted piperidines

Chiral aminoalkyl epoxyaziridine 1 is synthesized in high yield and diastereoselectivity from L-serine. Ring opening of epoxyaziridine I with primary amines is carried out with total chemo- and regioselectivity, affording chiral polyfunctionalized piperid