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Boronic acid, [2-(chloromethyl)phenyl]-

Base Information
  • Chemical Name:Boronic acid, [2-(chloromethyl)phenyl]-
  • CAS No.:374551-13-0
  • Molecular Formula:C7H8BClO2
  • Molecular Weight:170.403
  • Hs Code.:
  • Mol file:374551-13-0.mol
Boronic acid, [2-(chloromethyl)phenyl]-

Synonyms:

Suppliers and Price of Boronic acid, [2-(chloromethyl)phenyl]-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 1 raw suppliers
Chemical Property of Boronic acid, [2-(chloromethyl)phenyl]-
Chemical Property:
  • Melting Point:147 °C (diethyl ether) 
  • PSA:40.46000 
  • LogP:0.10520 
Purity/Quality:

95%-98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Boronic acid, [2-(chloromethyl)phenyl]-

There total 1 articles about Boronic acid, [2-(chloromethyl)phenyl]- 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-(chloromethyl)iodobenzene; With isopropylmagnesium chloride; In tetrahydrofuran; at -20 - -10 ℃; for 2h;
With Triisopropyl borate; In tetrahydrofuran; at -78 - 20 ℃;
With hydrogenchloride; water; In tetrahydrofuran;
DOI:10.1021/ol8006887
Guidance literature:
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; sodium carbonate; In 1,3-dioxane; water; at 50 ℃; for 20h; Inert atmosphere;
DOI:10.1021/ol8006887
Guidance literature:
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; sodium carbonate; In 1,3-dioxane; water; at 50 ℃; for 20h; regioselective reaction; Inert atmosphere;
DOI:10.1021/ol8006887
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