88243-77-0

Basic information

• Product Name: S-BENZYL-L-CYSTEINOL)
• Synonyms: 1-Propanol,2-amino-3-[(phenylmethyl)thio]-, (S)-;[(S)-2-Hydroxy-1-[[(phenylmethyl)thio]methyl]ethyl]amine
• CAS NO: 88243-77-0
• Molecular Formula: C₁₀H₁₅NOS
• Molecular Weight: 197.3
• Mol File: 88243-77-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: S-BENZYL-L-CYSTEINOL)(CAS DataBase Reference)
• NIST Chemistry Reference: S-BENZYL-L-CYSTEINOL)(88243-77-0)
• EPA Substance Registry System: S-BENZYL-L-CYSTEINOL)(88243-77-0)

Safety Data

• Hazardous Substances Data: 88243-77-0(Hazardous Substances Data)

Upstream product

• 3054-01-1 (D)-2-Amino-3-(benzylthio)propanoic acid 

Downstream Products

• 1201814-10-9 (S)-di-tert-butyl 2,2'-(1-(benzylthio)-3-hydroxypropan-2-ylazanediyl)diacetate 

Relevant articles and documents

Asymmetric Synthesis Using Chirally Modified Borohydrides. Part 1. Enantioselective Reduction of Aromatic Ketones with the Reagent Prepared from Borane and (S)-Valinol

The asymmetric reduction of aromatic ketones with the reagents prepared from borane and chiral aminoalcohols was studied under various conditions.The ratio of borane to (S)-valinol was found to be optimum at 2-3:1, when up to 65-73percent selectivity was obtained in the reduction of n-propyl phenyl ketone.The amino-alkoxy-amine-boranes (2) and/or (3) were tentatively proposed as the reaction species responsible for asymmetric induction.