228850-43-9

Basic information

• Product Name: [(1S,2S)-1-Benzyl-3-((2S,3S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butylsulfanyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester
• Synonyms: [(1S,2S)-1-Benzyl-3-((2S,3S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butylsulfanyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester
• CAS NO: 228850-43-9
• Molecular Weight: 560.755
• Mol File: 228850-43-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(1S,2S)-1-Benzyl-3-((2S,3S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butylsulfanyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(1S,2S)-1-Benzyl-3-((2S,3S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butylsulfanyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester(228850-43-9)
• EPA Substance Registry System: [(1S,2S)-1-Benzyl-3-((2S,3S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butylsulfanyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester(228850-43-9)

Safety Data

• Hazardous Substances Data: 228850-43-9(Hazardous Substances Data)

Upstream product

• 98760-08-8 (1-oxiranyl-2-phenylethyl)carbamic acid tert-butyl ester 
• 149451-80-9 (2S,3S)-3-(t-butoxycarbonylamino)-4-phenylbutane-1,2-diol 

Downstream Products

• 231307-22-5 C₃₆H₅₂N₂O₈S 
• 231307-28-1 C₃₆H₅₂N₂O₆ 
• 231307-19-0 C₃₆H₅₂N₂O₆S 

Relevant articles and documents

A convergent, stereocontrolled synthesis of C2-symmetrical and pseudosymmetrical sulfur-tethered bis(amino alcohols)

The totally enantiocontrolled preparation of C2-symmetrical and pseudosymmetrical sulfur-tethered bis(amino alcohols) from anti-3-amino-1,2- alkane diols is described. The key step in the synthetic procedure involves the use of triphenylsilanethiol as a sulfide or hydrogenosulfide equivalent in the regioselective nucleophilic ring opening of both anti- and syn- aminoalkyl epoxides.