152037-57-5

Basic information

• Product Name: (3R,5R)-3-{(2S,13S)-2-(tert-Butyl-dimethyl-silanyloxy)-13-hydroxy-13-[(2S,5S,2'S,5'S)-5'-((R)-1-hydroxy-undecyl)-octahydro-[2,2']bifuranyl-5-yl]-trideca-8,10-diynyl}-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one
• CAS NO: 152037-57-5
• Molecular Weight: 839.306
• Mol File: 152037-57-5.mol

Chemical Properties

• CAS DataBase Reference: (3R,5R)-3-{(2S,13S)-2-(tert-Butyl-dimethyl-silanyloxy)-13-hydroxy-13-[(2S,5S,2'S,5'S)-5'-((R)-1-hydroxy-undecyl)-octahydro-[2,2']bifuranyl-5-yl]-trideca-8,10-diynyl}-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,5R)-3-{(2S,13S)-2-(tert-Butyl-dimethyl-silanyloxy)-13-hydroxy-13-[(2S,5S,2'S,5'S)-5'-((R)-1-hydroxy-undecyl)-octahydro-[2,2']bifuranyl-5-yl]-trideca-8,10-diynyl}-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one(152037-57-5)
• EPA Substance Registry System: (3R,5R)-3-{(2S,13S)-2-(tert-Butyl-dimethyl-silanyloxy)-13-hydroxy-13-[(2S,5S,2'S,5'S)-5'-((R)-1-hydroxy-undecyl)-octahydro-[2,2']bifuranyl-5-yl]-trideca-8,10-diynyl}-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one(152037-57-5)

Safety Data

• Hazardous Substances Data: 152037-57-5(Hazardous Substances Data)

Upstream product

• 152037-54-2 (3R,5R)-3-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-9-trimethylsilanyl-non-8-ynyl]-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one 
• 152037-55-3 (3R,5R)-3-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-non-8-ynyl]-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one 
• 152037-52-0 Trimethyl-((S)-7-oxiranyl-hept-1-ynyl)-silane 
• 152037-58-6 (S)-Non-8-yne-1,2-diol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 115338-23-3 dilithiated phenylthioacetic acid 
• 152037-56-4 (3R,5R)-3-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-9-iodo-non-8-ynyl]-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one 

Relevant articles and documents

Synthesis of (-)-bullatacin: The enantiomer of a potent, antitumor, 4-hydroxylated, Annonaceous acetogenin

Synthesis of the title compound represents the first construction of any of these potent, antitumor Annonaceous acetogenins with the entire relative stereochemistry in place. Palladium(0)-mediated crossed diyne coupling and the use of three, natural, α-hy