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1-Bromo-2-methylcyclopentane

Base Information Edit
  • Chemical Name:1-Bromo-2-methylcyclopentane
  • CAS No.:31201-11-3
  • Molecular Formula:C6H11Br
  • Molecular Weight:163.057
  • Hs Code.:
  • European Community (EC) Number:867-682-7
  • Mol file:31201-11-3.mol
1-Bromo-2-methylcyclopentane

Synonyms:1-bromo-2-methylcyclopentane;31201-11-3;starbld0043041;SCHEMBL8163630;MFCD16092391;AKOS005266592;AKOS017439756;EN300-233858

Suppliers and Price of 1-Bromo-2-methylcyclopentane
Supply Marketing:Edit
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
Total 3 raw suppliers
Chemical Property of 1-Bromo-2-methylcyclopentane Edit
Chemical Property:
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:162.00441
  • Heavy Atom Count:7
  • Complexity:61.2
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1CCCC1Br
Technology Process of 1-Bromo-2-methylcyclopentane

There total 2 articles about 1-Bromo-2-methylcyclopentane 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 bromine; In tetrachloromethane; at 20 ℃; Yield given. Further byproducts given. Yields of byproduct given; Irradiation;
Guidance literature:
Multi-step reaction with 2 steps
1: ethanol / Erwaermen des erhaltenen Reaktionsprodukts mit wss.-aethanol. Kalilauge
2: 160 - 170 °C
With ethanol;
upstream raw materials:

bicyclo[3.1.0]hexane

Downstream raw materials:

2-(2-methyl-cyclopentyl)-4-phenyl-butyric acid

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