2-(2-Bromoethyl)oxolane

Base Information

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

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:

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

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:: 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:

Reference yield:

: 133243-93-3
2-(tetrahydrofuran-2-yl)ethyl methanesulfonate

: 1050493-67-8
2-(2-bromoethyl)oxolane

Guidance literature:: With lithium bromide; In acetone; for 3h; Heating / reflux;

Reference yield:

: 33606-34-7
(2-(tetrahydro-furan-2-yl)-ethanol)

: 1050493-67-8
2-(2-bromoethyl)oxolane

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;

Reference yield:

: 2434-02-8,139456-82-9
ethyl tetrahydrofuran-2-acetate

: 1050493-67-8
2-(2-bromoethyl)oxolane

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;