1285721-50-7

Basic information

• Product Name: C₂₃H₃₃NO₄S
• Synonyms: C₂₃H₃₃NO₄S
• CAS NO: 1285721-50-7
• Molecular Weight: 419.585
• Mol File: 1285721-50-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₃H₃₃NO₄S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₃H₃₃NO₄S(1285721-50-7)
• EPA Substance Registry System: C₂₃H₃₃NO₄S(1285721-50-7)

Safety Data

• Hazardous Substances Data: 1285721-50-7(Hazardous Substances Data)

Upstream product

• 58577-87-0 O-benzyl-L-serinol 
• 4726-96-9 O-Benzyl-L-serine 
• 2043-61-0 cyclohexanecarbaldehyde 
• 1285721-08-5 C₁₅H₁₉NO₃S 
• 1285721-06-3 C₁₇H₂₅NO₅S 

Downstream Products

• 1195780-69-8 C₁₉H₂₃F₃O₄ 
• 115362-12-4 (-)-(2S,3S)-2,3-epoxy-3-cyclohexyl-1-propanol 

Relevant articles and documents

Cyclic sulfur ylides derived from gleason-type chiral auxiliaries for the asymmetric synthesis of epoxy amides

Gleason-type chiral auxiliaries were used for the synthesis of a novel class of sulfonium salts, obtained via methylation of the sulfide with Meerwein's salt. The salts were reacted with aldehydes under basic conditions to provide epoxy amides, which were reduced to their corresponding epoxy alcohols in excellent enantiomeric excesses. Interestingly, it was feasible to synthesize both enantiomeric epoxy alcohols depending on which of the sulfonium salts, prepared from L-amino acids (6 and 9 from L-valine or 15 and 16 from L-serine) was employed.