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3-Bromo-2-hydroxyphenyl boronic acid

Base Information
  • Chemical Name:3-Bromo-2-hydroxyphenyl boronic acid
  • CAS No.:89488-24-4
  • Molecular Formula:C6H6 B Br O3
  • Molecular Weight:216.827
  • Hs Code.:
  • Mol file:89488-24-4.mol
3-Bromo-2-hydroxyphenyl boronic acid

Synonyms:3-Bromo-2-hydroxyphenyl boronic acid

Suppliers and Price of 3-Bromo-2-hydroxyphenyl boronic acid
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
  • AOBChem
  • 3-Bromo-2-hydroxyphenylboronicacid 95%
  • 10g
  • $ 436.00
  • American Custom Chemicals Corporation
  • 3-BROMO-2-HYDROXYPHENYL BORONIC ACID 95.00%
  • 5MG
  • $ 499.58
  • Alichem
  • 3-Bromo-2-hydroxyphenylboronicacid
  • 1g
  • $ 1519.80
  • Alichem
  • 3-Bromo-2-hydroxyphenylboronicacid
  • 500mg
  • $ 782.40
  • Alichem
  • 3-Bromo-2-hydroxyphenylboronicacid
  • 250mg
  • $ 504.00
Total 22 raw suppliers
Chemical Property of 3-Bromo-2-hydroxyphenyl boronic acid
Chemical Property:
  • PSA:60.69000 
  • LogP:-0.16550 
Purity/Quality:

98% *data from raw suppliers

3-Bromo-2-hydroxyphenylboronicacid 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3-Bromo-2-hydroxyphenyl boronic acid

There total 4 articles about 3-Bromo-2-hydroxyphenyl boronic acid 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:
2,6-dibromophenol; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
Trimethyl borate; In tetrahydrofuran; hexane; for 2h;
Guidance literature:
With chloro-trimethyl-silane; sodium iodide; In acetonitrile; at 0 - 20 ℃;
DOI:10.1016/j.tet.2013.03.016
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / dichloromethane / 7 h / 0 °C / Inert atmosphere
2.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C / Inert atmosphere
2.2: -78 - 20 °C / Inert atmosphere
3.1: sodium iodide; chloro-trimethyl-silane / acetonitrile / 0 - 20 °C
With n-butyllithium; chloro-trimethyl-silane; triethylamine; sodium iodide; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1016/j.tet.2013.03.016
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