210104-26-0

Basic information

• Product Name: (S)-3-((1R,2S)-2-Hydroxy-1-methyl-propoxy)-5-phenyl-pent-4-ynethioic acid S-tert-butyl ester
• Synonyms: (S)-3-((1R,2S)-2-Hydroxy-1-methyl-propoxy)-5-phenyl-pent-4-ynethioic acid S-tert-butyl ester
• CAS NO: 210104-26-0
• Molecular Weight: 334.48
• Mol File: 210104-26-0.mol

Chemical Properties

• CAS DataBase Reference: (S)-3-((1R,2S)-2-Hydroxy-1-methyl-propoxy)-5-phenyl-pent-4-ynethioic acid S-tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-((1R,2S)-2-Hydroxy-1-methyl-propoxy)-5-phenyl-pent-4-ynethioic acid S-tert-butyl ester(210104-26-0)
• EPA Substance Registry System: (S)-3-((1R,2S)-2-Hydroxy-1-methyl-propoxy)-5-phenyl-pent-4-ynethioic acid S-tert-butyl ester(210104-26-0)

Safety Data

• Hazardous Substances Data: 210104-26-0(Hazardous Substances Data)

Upstream product

• 63584-47-4 (1-tert-butylsulfanyl-vinyloxy)trimethylsilane 
• 195374-93-7 rel-(2S,3S,4R)-4,5-dimethyl-2-phenylethylnyl-1,3-dioxolane 
• 6142-95-6 phenylpropargyl aldehyde diethyl acetal 
• 513-85-9 2.3-butanediol 

Relevant articles and documents

Desymmetrization of meso-1,2-diols via chiral oxazaborolidine-mediated ring-cleavage of acetal derivatives with silyl ketene S,O-acetal

Desymmetrization of meso-1,2-diols leading to enantiomerically enriched MOM and MEM ethers is realized via chiral oxazaborolidine-mediated enantioselective ring-cleavage reaction of the acetal derivatives with silyl ketene S,O-acetal.