1361966-86-0

Basic information

• Product Name: (E)-N-(4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butan-2-ylidene)-1-phenylmethanamine
• Synonyms: (E)-N-(4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butan-2-ylidene)-1-phenylmethanamine
• CAS NO: 1361966-86-0
• Molecular Weight: 393.334
• Mol File: 1361966-86-0.mol

Chemical Properties

• CAS DataBase Reference: (E)-N-(4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butan-2-ylidene)-1-phenylmethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-(4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butan-2-ylidene)-1-phenylmethanamine(1361966-86-0)
• EPA Substance Registry System: (E)-N-(4-(4-methoxyphenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butan-2-ylidene)-1-phenylmethanamine(1361966-86-0)

Safety Data

• Hazardous Substances Data: 1361966-86-0(Hazardous Substances Data)

Upstream product

• 73183-34-3 bis(pinacol)diborane 

Relevant articles and documents

Catalytic 1,3-difunctionalisation of organic backbones through a highly stereoselective, one-pot, boron conjugate-addition/reduction/oxidation process

A simple one-pot, three-step synthetic route to chiral 1,3-amino alcohols and 1,3-diols has been established. Considering the overall stereocontrol of the synthetic protocol, the first and key step is an enantioselective β-boration of α,β-unsaturated imin