1457998-45-6

Basic information

• Product Name: C₂₈H₃₄F₃NO₃SSi
• Synonyms: C₂₈H₃₄F₃NO₃SSi
• CAS NO: 1457998-45-6
• Molecular Weight: 549.73
• Mol File: 1457998-45-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₈H₃₄F₃NO₃SSi(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₃₄F₃NO₃SSi(1457998-45-6)
• EPA Substance Registry System: C₂₈H₃₄F₃NO₃SSi(1457998-45-6)

Safety Data

• Hazardous Substances Data: 1457998-45-6(Hazardous Substances Data)

Upstream product

• 131744-19-9 (4S)-4-benzyl-1,3-oxazolidine-2-thione 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 1457998-44-5 C₂₂H₂₀F₃NO₃S 

Downstream Products

• 1457998-49-0 C₂₂H₃₁F₃O₃Si 
• 1457998-55-8 C₂₂H₃₁F₃O₃Si 
• 1457998-54-7 C₂₂H₃₃F₃O₅Si 
• 1457998-46-7 C₁₈H₂₇F₃O₂Si 
• 131744-19-9 (4S)-4-benzyl-1,3-oxazolidine-2-thione 
• 1457998-47-8 C₁₈H₂₆F₃IOSi 

Relevant articles and documents

Total synthesis of γ-trifluoromethylated analogs of goniothalamin and their derivatives

An efficient method for the construction of chiral γ- trifluoromethylated α,β-unsaturated δ-lactone, a widely existing pharmacophore, has been developed and successfully applied for synthesis of γ-trifluoromethylated goniothalamins. The key steps included Evans-Aldol reaction of chiral titanium enolate of α-CF3 imide, Wittig olefination and lactonization. The transformation of γ-trifluoromethylated α,β-unsaturated δ-lactone to a series of trifluoromethylated styryllactones was also investigated.