662168-51-6

Basic information

• Product Name: 4-Nonanol, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-6-(phenylmethylene)-, (4R,6E,8R)-
• CAS NO: 662168-51-6
• Molecular Formula: C23H40O2Si
• Molecular Weight: 376.655
• Mol File: 662168-51-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-Nonanol, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-6-(phenylmethylene)-, (4R,6E,8R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Nonanol, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-6-(phenylmethylene)-, (4R,6E,8R)-(662168-51-6)
• EPA Substance Registry System: 4-Nonanol, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-8-methyl-6-(phenylmethylene)-, (4R,6E,8R)-(662168-51-6)

Safety Data

• Hazardous Substances Data: 662168-51-6(Hazardous Substances Data)

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 662168-57-2 (+)-(4S)-isopropyl-3-[(2R)-methyl-5-phenylpent-4-ynoyl]oxazolidin-2-one 
• 662168-58-3 (+)-(2R)-methyl-5-phenylpent-4-yn-1-ol 
• 1794-48-5 1-bromo-3-phenylprop-2-yne 
• 139406-51-2 (R)-2-propylethylene oxide 
• 662168-50-5 (+)-1-(tert-butyldimethylsilanyloxy)-(2R)-methyl-5-phenyl-4-pentyne 

Downstream Products

• 662168-56-1 (-)-11,15-dibenzylidene-(14S)-hydroxy-(6S,13R,19R)-trimethyl-(9R)-propyl-8,20-dioxabicyclo[15.2.1]icosan-7-one 
• 662168-64-1 (+)-11,15-dibenzylidene-(14S)-(tert-butyldimethylsilanyloxy)-(6S,13R,19R)-trimethyl-(9R)-propyl-8,20-dioxaicyclo[15.2.1]icosane-7-one 
• 662168-55-0 (+)-(2S)-methyl-6-[(3S)-methyl-(5R)-(3-phenylprop-2-ynyl)tetrahydrofuran-(2S)-yl]hexanoic acid 3-benzylidene-(5R)-methyl-6-oxo-(1R)-propylhexyl ester 
• 662168-63-0 (+)-(2S)-methyl-6-[(3S)-methyl-(5R)-(3-phenylprop-2-ynyl)tetrahydrofuran-(2S)-yl]hexanoic acid 3-benzylidene-6-hydroxy-(5R)-methyl-(1R)-propylhexyl ester 

Relevant articles and documents

Total syntheses of amphidinolides T1 and T4 via catalytic, stereoselective, reductive macrocyclizations

Described in this work are total syntheses of amphidinolides T1 and T4 using two nickel-catalyzed reductive coupling reactions of alkynes, with an epoxide in one case (intermolecular) and with an aldehyde in another (intramolecular). The latter was used t