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4-BROMOBENZYL CYCLOHEXYL ETHER

Base Information
  • Chemical Name:4-BROMOBENZYL CYCLOHEXYL ETHER
  • CAS No.:1250419-82-9
  • Molecular Formula:C13H17BrO
  • Molecular Weight:269.181
  • Hs Code.:
4-BROMOBENZYL CYCLOHEXYL ETHER

Synonyms:1-bromo-4-(cyclohexyloxymethyl)benzene

Suppliers and Price of 4-BROMOBENZYL CYCLOHEXYL ETHER
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
  • Crysdot
  • 1-Bromo-4-((cyclohexyloxy)methyl)benzene 97%
  • 5g
  • $ 1131.00
  • Crysdot
  • 1-Bromo-4-((cyclohexyloxy)methyl)benzene 97%
  • 1g
  • $ 414.00
Total 1 raw suppliers
Chemical Property of 4-BROMOBENZYL CYCLOHEXYL ETHER
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

1-Bromo-4-((cyclohexyloxy)methyl)benzene 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 4-BROMOBENZYL CYCLOHEXYL ETHER

There total 3 articles about 4-BROMOBENZYL CYCLOHEXYL ETHER 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 boron trifluoride diethyl etherate; In dichloromethane; at 0 ℃; regioselective reaction; Inert atmosphere;
DOI:10.1021/ja205174c
Guidance literature:
Multi-step reaction with 2 steps
1: dichloromethane / 0.08 h / 0 °C / Inert atmosphere
2: boron trifluoride diethyl etherate / dichloromethane / 0 °C / Inert atmosphere
With boron trifluoride diethyl etherate; In dichloromethane;
DOI:10.1021/ja205174c
Guidance literature:
Multi-step reaction with 2 steps
1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 24 h / 0 - 23 °C / Inert atmosphere
2: boron trifluoride diethyl etherate / dichloromethane / 0 °C / Inert atmosphere
With dmap; boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/ja205174c
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