1011287-43-6

Basic information

• Product Name: (1-(furan-3-yl)-2-((1S,8aS)-5,5,8a-trimethyl-2-methylidenedecahydronaphthalen-1-yl)ethoxy)triisopropylsilane
• Synonyms: (1-(furan-3-yl)-2-((1S,8aS)-5,5,8a-trimethyl-2-methylidenedecahydronaphthalen-1-yl)ethoxy)triisopropylsilane
• CAS NO: 1011287-43-6
• Molecular Weight: 458.8
• Mol File: 1011287-43-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1-(furan-3-yl)-2-((1S,8aS)-5,5,8a-trimethyl-2-methylidenedecahydronaphthalen-1-yl)ethoxy)triisopropylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(furan-3-yl)-2-((1S,8aS)-5,5,8a-trimethyl-2-methylidenedecahydronaphthalen-1-yl)ethoxy)triisopropylsilane(1011287-43-6)
• EPA Substance Registry System: (1-(furan-3-yl)-2-((1S,8aS)-5,5,8a-trimethyl-2-methylidenedecahydronaphthalen-1-yl)ethoxy)triisopropylsilane(1011287-43-6)

Safety Data

• Hazardous Substances Data: 1011287-43-6(Hazardous Substances Data)

Upstream product

• 216011-55-1 (5S,9S,10S)-15,16-epoxy-12-hydroxy-labda-8⁽¹⁷⁾-13⁽¹⁶⁾,14-triene 
• 80522-42-5 triisopropylsilyl trifluoromethanesulfonate 

Relevant articles and documents

Synthesis of (+)-zerumin B using a regioselective singlet oxygen furan oxidation

(Chemical Equation Presented) A short and efficient synthesis of the antitumor diterpenoid (+)-zerumin B has been accomplished starting from (+)-sclareolide. At the heart of the synthetic strategy lies the regioselective formation of the α-substituted γ-hydroxybutenolide moiety of zerumin B. This was achieved by means of a [1,4] O→C triisopropylsilyl migration followed by singlet oxygen (1O2) oxidation of the resulting 2-triisopropylsilyl-3-(α-hydroxy)alkylfuran.