155220-76-1

Basic information

• Product Name: (S)-1-phenyl-2-benzylaminoethylamine
• Synonyms: (S)-1-phenyl-2-benzylaminoethylamine
• CAS NO: 155220-76-1
• Molecular Weight: 226.321
• Mol File: 155220-76-1.mol

Chemical Properties

• CAS DataBase Reference: (S)-1-phenyl-2-benzylaminoethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-phenyl-2-benzylaminoethylamine(155220-76-1)
• EPA Substance Registry System: (S)-1-phenyl-2-benzylaminoethylamine(155220-76-1)

Safety Data

• Hazardous Substances Data: 155220-76-1(Hazardous Substances Data)

Upstream product

• 5491-18-9 (S)-N-(benzyloxycarbonyl)phenylglycine 
• 2935-35-5 (S)-2-phenylglycine 
• 155322-81-9 (S)-2-amino-N-benzyl-2-phenylacetamide 

Downstream Products

• 155322-82-0 (3R,5S,8aS)-1-Benzyl-5-methyl-3-phenyl-octahydro-imidazo[1,2-a]pyridine 
• 155220-83-0 (3S,5R,8aR)-1-Benzyl-5-methyl-3-phenyl-octahydro-imidazo[1,2-a]pyridine 
• 155220-85-2 (3S,5R,8aR)-1-Benzyl-5-ethyl-3-phenyl-octahydro-imidazo[1,2-a]pyridine 
• 175792-78-6 (3S,5S,7R,7aS)-1-benzyl-5,7-bis(tert-butoxycarbonyl)-3-phenylhexahydropyrrolo[1,2-a]imidazole 
• 175792-77-5 (3S,5S,7R,7aS)-1-benzyl-5-tert-butoxycarbonyl-7-methoxycarbonyl-3-phenylhexahydropyrrolo[1,2-a]imidazole 
• 175792-75-3 (3S,5S,7R,7aS)-1-benzyl-5-tert-butoxycarbonyl-7-methoxycarbonyl-7-methyl-3-phenylhexahydropyrrolo[1,2-a]imidazole 
• 175792-71-9 (S)-1-benzyl-4-phenyl-4,5-dihydroimidazole 

Relevant articles and documents

Ruthenium Pybox-Catalyzed Enantioselective Intramolecular C-H Amination of Sulfamoyl Azides en Route to Chiral Vicinal Diamines

Enantioselective C(sp3)-H aminations allow an efficient access to nonracemic chiral amines. This work reports the catalytic asymmetric synthesis of chiral 1,2,5-thiadiazolidine-1,1-dioxides by an enantioselective ring-closing 1,5-C-H amination of sulfamoy

A new route to homochiral piperidines

The synthesis of an enantiomeric pair of enaminoesters from phenylglycine is described. Conjugate addition to α,β-enones, reductive cyclization-fragmentation to octahydroimidazopyridines and further reduction to remove the auxiliary atoms, completes a new route to homochiral piperidines in which the enaminoesters function as homochiral 'ethanal enamines'.