783322-43-0

Basic information

• Product Name: 3-Buten-2-ol, 1-(phenylthio)-, (2S)-
• CAS NO: 783322-43-0
• Molecular Formula: C10H12OS
• Molecular Weight: 180.271
• Mol File: 783322-43-0.mol

Chemical Properties

• CAS DataBase Reference: 3-Buten-2-ol, 1-(phenylthio)-, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Buten-2-ol, 1-(phenylthio)-, (2S)-(783322-43-0)
• EPA Substance Registry System: 3-Buten-2-ol, 1-(phenylthio)-, (2S)-(783322-43-0)

Safety Data

• Hazardous Substances Data: 783322-43-0(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 138332-13-5 2-hydroxy-3-butenyl-4-methyl-1-benzenesulfonate 

Downstream Products

• 783322-56-5 [(S)-1-((R)-Benzenesulfinylmethyl)-allyloxy]-tert-butyl-diphenyl-silane 
• 783322-55-4 [(S)-1-((S)-Benzenesulfinylmethyl)-allyloxy]-tert-butyl-diphenyl-silane 
• 881309-80-4 C₁₇H₁₉NO₃S₂ 

Relevant articles and documents

Stereoselective preparation of a key intermediate toward the synthesis of nelfinavir

A stereoselective synthesis of an intermediate that can be elaborated into the potent HTV-protease inhibitor, nelfinavir, is described. The key step of the reaction sequence is the stereoselective preparation of a bromosulfonamide from an olefin using the

A stereoselective synthesis of the hexahydroazepine core of (-)-balanol

A stereoselective synthesis of the hexahydroazepine core of (-)-balanol is described. The key step of the route includes the bromosulfonamidation of an olefin using the intramolecular sulfilimine group as the nucleophile and the Pummerer ene reaction.