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3-methyl-1-cyclohexen-1-ylboronic acid pinacol ester

Base Information
  • Chemical Name:3-methyl-1-cyclohexen-1-ylboronic acid pinacol ester
  • CAS No.:1046831-99-5
  • Molecular Formula:C13H23BO2
  • Molecular Weight:222.135
  • Hs Code.:
3-methyl-1-cyclohexen-1-ylboronic acid pinacol ester

Synonyms:3-methyl-1-cyclohexen-1-ylboronic acid pinacol ester

Suppliers and Price of 3-methyl-1-cyclohexen-1-ylboronic 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
  • 4,4,5,5-Tetramethyl-2-(5-methyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane
  • 250mg
  • $ 165.00
  • Chemenu
  • 4,4,5,5-Tetramethyl-2-(5-methylcyclohex-1-en-1-yl)-1,3,2-dioxaborolane 95+%
  • 1g
  • $ 2059.00
Total 3 raw suppliers
Chemical Property of 3-methyl-1-cyclohexen-1-ylboronic acid pinacol ester
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

4,4,5,5-Tetramethyl-2-(5-methyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 4,4,5,5-Tetramethyl-2-(5-methyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane is a reagent that is used in the preparation of azaindole derivatives as c-Jun N-terminal kinase inhibitors. These inhibitors are useful in the treatment of neurodegenerative disorders, inflammatory diseases and autoimmune diseases.
Technology Process of 3-methyl-1-cyclohexen-1-ylboronic acid pinacol ester

There total 3 articles about 3-methyl-1-cyclohexen-1-ylboronic 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:
3-Methylcyclohexanon-tosylhydrazon; With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; In hexane; at -78 - 25 ℃; for 3h;
2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; In hexane; at -78 ℃;
DOI:10.1039/d0gc01514h
Guidance literature:
Multi-step reaction with 2 steps
1.1: methanol / 2 h / 70 °C / Reflux
2.1: N,N,N,N,-tetramethylethylenediamine; n-butyllithium / hexane / 3 h / -78 - 25 °C
2.2: -78 °C
With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; In methanol; hexane;
DOI:10.1039/d0gc01514h
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