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3,4-Dibromophenylboronic acid,pinacol ester

Base Information
  • Chemical Name:3,4-Dibromophenylboronic acid,pinacol ester
  • CAS No.:1075719-78-6
  • Molecular Formula:C12H15BBr2O2
  • Molecular Weight:361.869
  • Hs Code.:2934999090
  • Mol file:1075719-78-6.mol
3,4-Dibromophenylboronic acid,pinacol ester

Synonyms:3,4-Dibromophenylboronic acid,pinacol ester;2-(3,4-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Suppliers and Price of 3,4-Dibromophenylboronic acid,pinacol ester
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 3,4-Dibromophenylboronicacid,pinacolester
  • 50mg
  • $ 50.00
  • Crysdot
  • 2-(3,4-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 95+%
  • 5g
  • $ 847.00
  • Alichem
  • 2-(3,4-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 5g
  • $ 889.20
  • AK Scientific
  • 3,4-Dibromophenylboronicacidpinacolester
  • 5g
  • $ 1251.00
Total 12 raw suppliers
Chemical Property of 3,4-Dibromophenylboronic acid,pinacol ester
Chemical Property:
  • PSA:18.46000 
  • LogP:3.51080 
  • Storage Temp.:2-8°C 
  • Solubility.:Dichloromethane; Ethyl Acetate; Tetrahydrofuran 
Purity/Quality:

98%min *data from raw suppliers

3,4-Dibromophenylboronicacid,pinacolester *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 3,4-Dibromophenylboronic acid, pinacol ester
Technology Process of 3,4-Dibromophenylboronic acid,pinacol ester

There total 6 articles about 3,4-Dibromophenylboronic acid,pinacol ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; cyclopentyl methyl ether; 1,1'-di(pyridin-2-yl)-1,1',3,3'-tetrahydro-2,2'-bibenzo[d][1,3,2]diazaborole; at 80 ℃; for 16h; Schlenk technique; Inert atmosphere;
DOI:10.1021/jacs.5b05252
Guidance literature:
With [Ir(C8H12)(OCH3)]2; 4,4'-di-tertbutylpyridine; In further solvent(s); (N2); heating mixt. of iridium compd., bipyridine deriv., benzene deriv., dodecane and silylborane deriv. at 80°C for 4 h; cooling to room temp., chromy. (silica gel, diethyl ether in hexane (gradient from 0% to 5%)), NMR;
DOI:10.1021/om800696d
Guidance literature:
1,2-dibromo-4-iodobenzene; With isopropylmagnesium chloride; In tetrahydrofuran; at -78 ℃; for 3h; Inert atmosphere;
2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; In tetrahydrofuran; at -78 - 25 ℃; Inert atmosphere;
DOI:10.1002/ejoc.201001217
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