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2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%

Base Information
  • Chemical Name:2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%
  • CAS No.:1223598-41-1
  • Molecular Formula:C13H18BN3O2
  • Molecular Weight:259.116
  • Hs Code.:
  • Mol file:1223598-41-1.mol
2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%

Synonyms:2-(2-(azidomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Suppliers and Price of 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%
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
  • 2-(2-(Azidomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 50mg
  • $ 55.00
  • Alfa Aesar
  • 2-(Azidomethyl)benzeneboronic acid pinacol ester, 95%
  • 1g
  • $ 66.30
  • Alfa Aesar
  • 2-(Azidomethyl)benzeneboronic acid pinacol ester, 95%
  • 5g
  • $ 247.00
  • AK Scientific
  • 2-(2-(Azidomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1g
  • $ 131.00
Total 4 raw suppliers
Chemical Property of 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

2-(2-(Azidomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95%

There total 5 articles about 2-(AzidoMethyl)benzeneboronic acid pinacol ester, 95% 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:
Multi-step reaction with 2 steps
1: acetonitrile / 4 h / 90 °C
2: dimethyl sulfoxide / 16 h / 20 °C
In dimethyl sulfoxide; acetonitrile;
DOI:10.1039/C6CC08534B
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