1512864-22-0

Basic information

• Product Name: 2,2'-(3-(2-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
• Synonyms: 2,2'-(3-(2-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
• CAS NO: 1512864-22-0
• Molecular Weight: 451.017
• Mol File: 1512864-22-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,2'-(3-(2-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-(3-(2-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)(1512864-22-0)
• EPA Substance Registry System: 2,2'-(3-(2-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)(1512864-22-0)

Safety Data

• Hazardous Substances Data: 1512864-22-0(Hazardous Substances Data)

Upstream product

• 107408-16-2 3-(o-bromophenyl)propanal 
• 1512864-11-7 C₁₆H₁₇BrN₂O₂S 
• 73183-34-3 bis(pinacol)diborane 
• 1074-15-3 1-bromo-2-(2-bromoethyl)benzene 
• 78782-17-9 4,4,5,5-tetramethyl-2-[(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]-1,3,2-dioxaborolane 
• 18698-97-0 ortho-bromophenylacetic acid 
• 339166-89-1 2,2'-(ethene-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane) 

Relevant articles and documents

Photoredox-Mediated Reaction of gem-Diborylalkenes: Reactivity Toward Diverse 1,1-Bisborylalkanes

The use of gem-diborylalkenes as radical-reactive groups is explored for the first time. These reactions provide an efficient and general method for the photochemical conversion of gem-diborylalkenes to rapidly access 1,1-bisborylalkanes. This method expl

Formal carbon insertion of n-tosylhydrazone into B-B and B-Si bonds: Gem-diborylation and gem-silylborylation of sp3 carbon

A convenient method is developed to synthesize 1,1-diboronates from the corresponding N-tosylhydrazones. This method is also applicable to synthesize 1-silyl-1-boron compounds. Meanwhile, derivatization and consecutive Pd-catalyzed cross-coupling reaction