310450-40-9

Basic information

• Product Name: (2R,3S,R_S)-N-(tert-butoxycarbonyl)-3-amino-1-(p-tolylsulfinyl)-2-butanol
• Synonyms: (2R,3S,R_S)-N-(tert-butoxycarbonyl)-3-amino-1-(p-tolylsulfinyl)-2-butanol
• CAS NO: 310450-40-9
• Molecular Weight: 327.445
• Mol File: 310450-40-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S,R_S)-N-(tert-butoxycarbonyl)-3-amino-1-(p-tolylsulfinyl)-2-butanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S,R_S)-N-(tert-butoxycarbonyl)-3-amino-1-(p-tolylsulfinyl)-2-butanol(310450-40-9)
• EPA Substance Registry System: (2R,3S,R_S)-N-(tert-butoxycarbonyl)-3-amino-1-(p-tolylsulfinyl)-2-butanol(310450-40-9)

Safety Data

• Hazardous Substances Data: 310450-40-9(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 310450-35-2 (3S,R_S)-N-(tert-butoxycarbonyl)-3-amino-1-(p-tolylsulfinyl)-2-butanone 
• 28875-17-4 (S)-N-(tert-butoxycarbonyl)alanine methyl ester 

Downstream Products

• 157394-45-1 (2S,3S)-N-(tert-butoxycarbonyl)-3-amino-2-butanol 

Relevant articles and documents

Synthesis of enantiomerically pure 2-amino alcohols from amino acids mediated by sulfoxides

Enantiomerically pure (R1,S2)- and (S1,S2)-2-amino alcohols can be easily synthesized by stereodivergent reduction of α'-(N-Boc)amino β-keto sulfoxides (easily synthesized from readily available N-Boc amino este