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2-(2-Bromoethyl)oxolane

Base Information Edit
  • Chemical Name:2-(2-Bromoethyl)oxolane
  • CAS No.:1050493-67-8
  • Molecular Formula:C6H11BrO
  • Molecular Weight:179.057
  • Hs Code.:
  • European Community (EC) Number:824-156-1
  • Mol file:1050493-67-8.mol
2-(2-Bromoethyl)oxolane

Synonyms:2-(2-bromoethyl)oxolane;2-(2-Bromoethyl)tetrahydrofuran;1050493-67-8;SCHEMBL2197276;GJDABTPRDFGPCR-UHFFFAOYSA-N;AKOS014489211;FT-0713437;EN300-169915

Suppliers and Price of 2-(2-Bromoethyl)oxolane
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
  • TRC
  • 2-(2-Bromoethyl)oxolane
  • 100mg
  • $ 350.00
  • AK Scientific
  • 2-(2-Bromoethyl)tetrahydrofuran
  • 250mg
  • $ 567.00
Total 1 raw suppliers
Chemical Property of 2-(2-Bromoethyl)oxolane Edit
Chemical Property:
  • XLogP3:1.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:177.99933
  • Heavy Atom Count:8
  • Complexity:65.5
Purity/Quality:

95+% *data from raw suppliers

2-(2-Bromoethyl)oxolane *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CC(OC1)CCBr
Technology Process of 2-(2-Bromoethyl)oxolane

There total 3 articles about 2-(2-Bromoethyl)oxolane 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 lithium bromide; In acetone; for 3h; Heating / reflux;
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane / 16 h / 0 - 20 °C
2: lithium bromide / acetone / 3 h / Heating / reflux
With triethylamine; lithium bromide; In dichloromethane; acetone;
Guidance literature:
Multi-step reaction with 3 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 - 20 °C
1.2: 0 - 10 °C
2.1: triethylamine / dichloromethane / 16 h / 0 - 20 °C
3.1: lithium bromide / acetone / 3 h / Heating / reflux
With lithium aluminium tetrahydride; triethylamine; lithium bromide; In tetrahydrofuran; dichloromethane; acetone;
Refernces Edit
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