212965-33-8

Basic information

• Product Name: (S)-2-((S)-2-Hydroxy-2-phenyl-ethylsulfanyl)-1-phenyl-ethanol
• Synonyms: (S)-2-((S)-2-Hydroxy-2-phenyl-ethylsulfanyl)-1-phenyl-ethanol
• CAS NO: 212965-33-8
• Molecular Weight: 274.384
• Mol File: 212965-33-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-((S)-2-Hydroxy-2-phenyl-ethylsulfanyl)-1-phenyl-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-((S)-2-Hydroxy-2-phenyl-ethylsulfanyl)-1-phenyl-ethanol(212965-33-8)
• EPA Substance Registry System: (S)-2-((S)-2-Hydroxy-2-phenyl-ethylsulfanyl)-1-phenyl-ethanol(212965-33-8)

Safety Data

• Hazardous Substances Data: 212965-33-8(Hazardous Substances Data)

Upstream product

• 212965-35-0 Toluene-4-sulfonic acid (S)-2-(1-ethoxy-ethoxy)-2-phenyl-ethyl ester 
• 212965-31-6 (S)-(1-Ethoxy-ethoxy)-phenyl-acetic acid ethyl ester 
• 208458-94-0 (2S,4RS)-2-Phenyl-4-methyl-3,5-dioxaheptan-1-ol 
• 13704-09-1 (S)-(-)-ethyl mandelate 
• 40435-14-1 (S)-1-phenyl-2-(tosyloxy)ethanol 

Downstream Products

• 85996-23-2 rac-bis-1,2-(ethylsulfanyl)-1-phenylethane 
• 340168-19-6 (S,S)-(+)-bis(2-phenyl-2-chloroethyl)sulfide 

Relevant articles and documents

Novel synthesis of chiral, enantiomerically pure thiodiglycols and diglycols

Natural α-hydroxy acids have been converted in a sequence of O- protection, reduction, O-activation, thioether and ether formation and deprotection to chiral, non-racemic β,β'-dihydroxy thioethers 1a, 1b and ether 1c. Overall yields are excellent (75%). In an attempt to synthesize the respective dihydroxy ether 1d derived from mandelic acid 1,3-dioxolane derivatives 7 were obtained.