99315-43-2

Basic information

• Product Name: (3R,4S)-4-Benzyloxy-3-hydroxy-2-methylsulfanyl-pentanoic acid tert-butyl ester
• CAS NO: 99315-43-2
• Molecular Weight: 326.457
• Mol File: 99315-43-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,4S)-4-Benzyloxy-3-hydroxy-2-methylsulfanyl-pentanoic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4S)-4-Benzyloxy-3-hydroxy-2-methylsulfanyl-pentanoic acid tert-butyl ester(99315-43-2)
• EPA Substance Registry System: (3R,4S)-4-Benzyloxy-3-hydroxy-2-methylsulfanyl-pentanoic acid tert-butyl ester(99315-43-2)

Safety Data

• Hazardous Substances Data: 99315-43-2(Hazardous Substances Data)

Upstream product

• 81445-44-5 (S)-2-(benzyloxy)propanal 
• 102861-56-3 ((Z)-1-tert-Butoxy-2-methylsulfanyl-vinyloxy)-trimethyl-silane 
• 32368-18-6 α-thiomethoxyacetic acid tert-butyl ester 

Downstream Products

• 102861-57-4 tert-butyl (3S,4S)-3-(tert-butyl-dimethyl-silanyloxy)-4-(benzyloxy)pentanoate 

Relevant articles and documents

LEWIS ACID MEDIATED 1,2-ASYMETRIC lk-INDUCTION TO α-ALKOXYALDEHIDE: SYNTHESIS OF α-NONSUBSTITUTED β,γ-syn-DIHYDROXYKETONE AND ESTER

Lewis acid mediated reactions of methylthio substituted silyl enolate or ketene silyl acetal to α-alkoxyaldehyde give syn diols.A novel stereocontrolled synthesis of α-nonsubstituted β,γ-dihydroxyketone and ester is described.