4-(2-Bromopropyl)-1,2-dimethoxybenzene

Base Information

Chemical Name:4-(2-Bromopropyl)-1,2-dimethoxybenzene
CAS No.:19578-93-9
Molecular Formula:C11H15BrO2
Molecular Weight:259.143
Hs Code.:
DSSTox Substance ID:DTXSID501283733
Mol file:19578-93-9.mol

Synonyms:4-(2-bromopropyl)-1,2-dimethoxybenzene;19578-93-9;SCHEMBL3469321;UGTFRYYLKFTUMT-UHFFFAOYSA-N;DTXSID501283733;2-bromo-4,5-dimethoxypropylbenzene;AKOS012315887;CS-0302607;EN300-1897786

Suppliers and Price of 4-(2-Bromopropyl)-1,2-dimethoxybenzene

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
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price

Total 1 raw suppliers

Chemical Property of 4-(2-Bromopropyl)-1,2-dimethoxybenzene

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:258.02554
Heavy Atom Count:14
Complexity:163

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(CC1=CC(=C(C=C1)OC)OC)Br

Technology Process of 4-(2-Bromopropyl)-1,2-dimethoxybenzene

There total 4 articles about 4-(2-Bromopropyl)-1,2-dimethoxybenzene 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: 65.0%

: 93-15-2
1,2-dimethoxy-4-(2-propenyl)benzene

: 19578-93-9
1-(3,4-dimethoxyphenyl)-2-bromopropane

Guidance literature:: With hydrogen bromide; In acetic acid; at 0 ℃;

Reference yield:

: 97-53-0
4-allylguaiacol

: 19578-93-9
1-(3,4-dimethoxyphenyl)-2-bromopropane

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / K₂CO₃ / acetone / 6 h / Heating

2: 65 percent / HBr / acetic acid / 0 °C

With hydrogen bromide; potassium carbonate; In acetic acid; acetone;

Reference yield:

: 776-99-8
3,4-dimethoxyphenylacetone

: 19578-93-9
1-(3,4-dimethoxyphenyl)-2-bromopropane

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄ / bis-(2-methoxy-ethyl) ether

2: HBr, Py / benzene; petroleum ether

With pyridine; sodium tetrahydroborate; hydrogen bromide; In diethylene glycol dimethyl ether; Petroleum ether; benzene;