1202649-49-7

Basic information

• Product Name: (S)-N-tert-butoxycarbonyl-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-phenylethanamine
• Synonyms: (S)-N-tert-butoxycarbonyl-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-phenylethanamine
• CAS NO: 1202649-49-7
• Molecular Weight: 321.417
• Mol File: 1202649-49-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-N-tert-butoxycarbonyl-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-phenylethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-tert-butoxycarbonyl-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-phenylethanamine(1202649-49-7)
• EPA Substance Registry System: (S)-N-tert-butoxycarbonyl-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-phenylethanamine(1202649-49-7)

Safety Data

• Hazardous Substances Data: 1202649-49-7(Hazardous Substances Data)

Upstream product

• 1202649-48-6 (S)-N-benzyl-N-tert-butoxycarbonyl-1-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-phenylethanamine 

Downstream Products

• 149451-80-9 (2S,3S)-3-(t-butoxycarbonylamino)-4-phenylbutane-1,2-diol 

Relevant articles and documents

Expedient asymmetric synthesis of (2S,3S)-Boc-phenylalanine epoxide, a key intermediate for the synthesis of biologically active compounds

The asymmetric synthesis of (2S,3S)-3-(tert-butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane [(2S,3S)-Boc-phenylalanine epoxide] has been achieved in six steps and in 55% overall yield from the N-benzylimine derived from (R)-2,3-O-isopropylidene-glyceraldehy