229010-45-1

Basic information

• Product Name: tert-Butyl-[2-((1S,3R,4R)-3-isopropenyl-4-methyl-4-vinyl-cyclohexyl)-ethoxy]-dimethyl-silane
• CAS NO: 229010-45-1
• Molecular Weight: 322.607
• Mol File: 229010-45-1.mol

Chemical Properties

• CAS DataBase Reference: tert-Butyl-[2-((1S,3R,4R)-3-isopropenyl-4-methyl-4-vinyl-cyclohexyl)-ethoxy]-dimethyl-silane(CAS DataBase Reference)
• NIST Chemistry Reference: tert-Butyl-[2-((1S,3R,4R)-3-isopropenyl-4-methyl-4-vinyl-cyclohexyl)-ethoxy]-dimethyl-silane(229010-45-1)
• EPA Substance Registry System: tert-Butyl-[2-((1S,3R,4R)-3-isopropenyl-4-methyl-4-vinyl-cyclohexyl)-ethoxy]-dimethyl-silane(229010-45-1)

Safety Data

• Hazardous Substances Data: 229010-45-1(Hazardous Substances Data)

Upstream product

• 229010-43-9 (1S,2S,4R,5R)-2-<2-(tert-Butyldimethylsilyloxy)ethyl>-4-isopropenyl-5-methyl-5-vinylcyclohexanol 
• 229010-41-7 (1S,4R,5R)-5-Isopropenyl-1-methoxycarbonylmethyl-4-methyl-2-oxo-4-vinyl-cyclohexanecarboxylic acid ethyl ester 
• 229010-40-6 Methyl 2-<(1S,4R,5R)-5-isopropenyl-4-methyl-4-vinyl-2-oxocyclohexyl>acetate 
• 229010-42-8 (1S,2S,4R,5R)-2-(2-Hydroxy-ethyl)-4-isopropenyl-5-methyl-5-vinyl-cyclohexanol 
• 149404-72-8 (3R,4R)-3-Methyl-4-isopropenyl-3-vinylcyclohexanone 
• 202194-28-3 (1R,4R,5R)-5-Isopropenyl-4-methyl-2-oxo-4-vinyl-cyclohexanecarboxylic acid ethyl ester 
• 149404-74-0 (4R,5R)-1-Acetoxy-4-isopropenyl-5-methyl-5-vinylcyclohex-1-ene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 229010-44-0 dithiocarbonic acid O-{2-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-isopropenyl-5-methyl-5-vinyl-cyclohexyl} ester S-methyl ester 

Downstream Products

• 229010-46-2 2-<(1S,3R,4R)-(3-Isopropenyl-4-methyl-4-vinylcyclohexyl)>ethanol 
• 139579-30-9 lobatrientriol 
• 139579-31-0 lobatrienolide 
• 229010-37-1 Methyl 2-<(1S,3R,4R)-3-isopropenyl-4-methyl-4-vinylcyclohexyl>acetate 
• 229010-51-9 Methyl (5R)-2-<(1S,3R,4R)-3-isopropenyl-4-methyl-4-vinylcyclohexyl>-5,6-dihydroxy-6-methylheptanoate 
• 229010-50-8 Methyl 2-<(1S,3R,4R)-3-isopropenyl-4-methyl-4-vinylcyclohexyl>-4-<(5R)-2,2,4,4-tetramethyl-1,3-dioxolan-5-yl>butanoate 

Relevant articles and documents

Synthetic study of marine lobane diterpenes. Enantioselective syntheses of lobatrienolide and lobatrientriol from (+)-nopinone

Michiharu Kato,. The first enantioselective syntheses of highly oxygenated lobane diterpenes, (+)-lobatrienolide 4 and (+)-lobatrientriol 5, have been achieved, starting with (4R,5R)-1-acetoxy-4-isopropenyl-5-methyl-5-vinyl-cyclohex-1-ene 10b which itself has been prepared from (+)-nopinone 7 as a versatile building block toward the asymmetric synthesis of natural products.