2-Bromo-3-methoxy-butane

Base Information

Chemical Name:2-Bromo-3-methoxy-butane
CAS No.:24618-36-8
Molecular Formula:C₅H₁₁BrO
Molecular Weight:167.046
Hs Code.:
DSSTox Substance ID:DTXSID501313928

Synonyms:2-bromo-3-methoxybutane;24618-36-8;2-bromo-3-methoxy-butane;DTXSID501313928;EN300-323187

Suppliers and Price of 2-Bromo-3-methoxy-butane

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

Total 3 raw suppliers

Chemical Property of 2-Bromo-3-methoxy-butane

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:165.99933
Heavy Atom Count:7
Complexity:47.3

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C(C)Br)OC

Technology Process of 2-Bromo-3-methoxy-butane

There total 2 articles about 2-Bromo-3-methoxy-butane 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:

: 67-56-1
methanol

: 590-18-1
(Z)-2-Butene

: 5408-86-6
2,3-dibromobutane

: 24618-36-8
2-bromo-3-methoxy-butane

Guidance literature:: With sodium bromide; In methanol; at 25 ℃; Product distribution; electrolysis; regio-, chemo- and stereoselectivity of bromination; other 1,2-disubstituted cis-alkenes;
DOI:10.1021/jo00059a051

Reference yield:

: 67-56-1
methanol

: 624-64-6
trans-2-Butene

: 5408-86-6
2,3-dibromobutane

: 24618-36-8
2-bromo-3-methoxy-butane

Guidance literature:: With sodium bromide; In methanol; at 25 ℃; Product distribution; electrolysis; regio- ,stereo- and chemoselectivity of bromination; other 1,2-disubstituted trans-alkenes;
DOI:10.1021/jo00059a051