1417803-51-0

Basic information

• Product Name: (5S)-5-[(2S)-3-(tert-butyldiphenylsiloxy)-2-methylpropyl]furan-2(5H)-one
• Synonyms: (5S)-5-[(2S)-3-(tert-butyldiphenylsiloxy)-2-methylpropyl]furan-2(5H)-one
• CAS NO: 1417803-51-0
• Molecular Weight: 394.586
• Mol File: 1417803-51-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (5S)-5-[(2S)-3-(tert-butyldiphenylsiloxy)-2-methylpropyl]furan-2(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5S)-5-[(2S)-3-(tert-butyldiphenylsiloxy)-2-methylpropyl]furan-2(5H)-one(1417803-51-0)
• EPA Substance Registry System: (5S)-5-[(2S)-3-(tert-butyldiphenylsiloxy)-2-methylpropyl]furan-2(5H)-one(1417803-51-0)

Safety Data

• Hazardous Substances Data: 1417803-51-0(Hazardous Substances Data)

Upstream product

• 1417803-53-2 (2S,4S)-5-(tert-butyldiphenylsiloxy)-2-hydroxy-4-methylpentanal 
• 188945-44-0 ethyl 2-[bis(2-isopropylphenoxy)phosphoryl]acetate 
• 175272-36-3 (4R)-4-Benzyl-3-[(2S)-2-methyl-4-pentenoyl]-1,3-oxazolidin-2-one 

Downstream Products

• 1417803-56-5 C₂₇H₃₄O₂Si 
• 1417803-54-3 (4R,5S)-4-allyl-5-[(2S)-3-tert-butyldiphenylsiloxy-2-methylpropyl]dihydrofuran-2(3H)-one 
• 1417803-55-4 C₃₀H₄₄O₃Si₂ 

Relevant articles and documents

Asymmetric total syntheses of xanthatin and 11,13-dihydroxanthatin using a stereocontrolled conjugate allylation to γ-butenolide

The stereocontrolled conjugate allylation to an optically pure γ-butenolide provided direct and reliable access to a trans-fused series of xanthanolide sesquiterpenoids and allowed for the enantioselective total syntheses of xanthatin and 11,13-dihydroxanthatin to be efficiently achieved.