505094-29-1

Basic information

• Product Name: (4R,5R)-4,5-dicyclohexyl-2-[(1R)-1-methylpropyl]-1,3,2-dioxaborolane
• Synonyms: (4R,5R)-4,5-dicyclohexyl-2-[(1R)-1-methylpropyl]-1,3,2-dioxaborolane
• CAS NO: 505094-29-1
• Molecular Weight: 292.27
• Mol File: 505094-29-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4R,5R)-4,5-dicyclohexyl-2-[(1R)-1-methylpropyl]-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: (4R,5R)-4,5-dicyclohexyl-2-[(1R)-1-methylpropyl]-1,3,2-dioxaborolane(505094-29-1)
• EPA Substance Registry System: (4R,5R)-4,5-dicyclohexyl-2-[(1R)-1-methylpropyl]-1,3,2-dioxaborolane(505094-29-1)

Safety Data

• Hazardous Substances Data: 505094-29-1(Hazardous Substances Data)

Upstream product

• 152428-82-5 (4R,5R)-4,5-dicyclohexyl-2-methyl-1,3,2-dioxaborolane 
• 505094-28-0 (4R,5R)-2-Methyl-4,5-diphenyl-[1,3,2]dioxaborolane 
• 52340-78-0 (R,R)-hydroxybenzoin 
• 2386-64-3 ethylmagnesium chloride 
• 141550-15-4 (R,R)-1,2-dicyclohexylethanediol (S)-(1-chloroethyl)boronate 

Relevant articles and documents

Acyclic stereoselective boron alkylation reactions for the asymmetric synthesis of β-substituted α-amino acid derivatives

Optically active syn- or anti-β-substituted-α-amino acid derivatives are prepared in 94 to ≥99% ee and 66-98% ds by reaction of the Schiff base acetate of glycine tert-butyl ester with chiral, nonracemic B-alkyl-9-BBN derivatives in the presence of the Cinchona alkaloid, cinchonidine (CdOH) or cinchonine (CnOH), base, and lithium chloride. Copyright