105065-55-2

Basic information

• Product Name: (4S,5S)-4,5-dicyclohexyl-2-<(1S,2Z)-1-methyl-2-butenyl>-1,3,2-dioxaborolane
• CAS NO: 105065-55-2
• Molecular Weight: 304.281
• Mol File: 105065-55-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,5S)-4,5-dicyclohexyl-2-<(1S,2Z)-1-methyl-2-butenyl>-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-4,5-dicyclohexyl-2-<(1S,2Z)-1-methyl-2-butenyl>-1,3,2-dioxaborolane(105065-55-2)
• EPA Substance Registry System: (4S,5S)-4,5-dicyclohexyl-2-<(1S,2Z)-1-methyl-2-butenyl>-1,3,2-dioxaborolane(105065-55-2)

Safety Data

• Hazardous Substances Data: 105065-55-2(Hazardous Substances Data)

Upstream product

• 105065-54-1 (4S,5S)-2-dichloromethyl-4,5-dicyclohexyl-1,3,2-dioxaborolane 
• 917-54-4 methyllithium 
• 6524-17-0 (Z)-1-propenyllithium 

Downstream Products

• 161912-67-0 (3E,5R,6S,7E)-5-(4-methoxybenzyloxy)-4,6-dimethyl-3,7-nonadiene 
• 161912-63-6 (3R,4S,5E)-3-(4-methoxybenzyloxy)-2,4-dimethylhepta-1,5-diene 
• 161912-57-8 (2R,3S)-2-ethyl-3-<(1R,2S,3E)-1-(4-methoxybenzyloxy)-2-methyl-3-pentenyl>-3-methyl-1,4-dioxaspiro<4.4>nonane 
• 105065-56-3 (1R,2S,3E)-2-methyl-1-phenyl-3-penten-1-ol 
• 120850-91-1 (S,S)-(-)-1,2-dicyclohexyl-ethane-1,2-diol 
• 147033-15-6 (2E,4S,5R,6S,7R,8R,10R)-10-<(2R,4R,5S,6S)-6-<(2R,3S)-2-ethyl-3-methyl-1,4-dioxaspiro<4.4>nonan-3-yl>-4-<2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl>>-5,8-dihydroxy-7-(4-methoxybenzyloxy)-4,6,8-trimethyl-2-undecene 
• 160497-72-3 (E)-(1R,2S)-1-((2R,3S)-3-{(S)-1-[(2R,4S,5S,6R)-6-((2R,3R)-3-Ethyl-2-methyl-1,4-dioxa-spiro[4.4]non-2-yl)-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-ethyl}-2-methyl-oxiranyl)-2-methyl-pent-3-en-1-ol 
• 83587-15-9 (S)-2-Vinyl-cyclopropane-1,1-dicarboxylic acid bis-[(1S,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl] ester 

Relevant articles and documents

Stereoselective Synthesis of Alcohols, XXXI. - Stereoselective C-C Bond Formation Using Chiral Z-Pentenylboronates

Using 1,2-dicyclohexyl-1,2-ethanediol as chiral auxiliary, the enantiomerically pure Z-pentenylboronate 9c was obtained.Its addition to benzaldehyde proceeded with complete transfer of chirality to give the syn-E-homoallyl alcohol 11.The ability of the re