4-Allyloxybenzyl bromide

Base Information

Chemical Name:4-Allyloxybenzyl bromide
CAS No.:143116-30-7
Molecular Formula:C10H11BrO
Molecular Weight:227.101
Hs Code.:
European Community (EC) Number:860-505-4
DSSTox Substance ID:DTXSID80464404
Nikkaji Number:J2.255.567G
Wikidata:Q82289704
Mol file:143116-30-7.mol

Synonyms:4-allyloxybenzyl bromide;143116-30-7;1-(Bromomethyl)-4-prop-2-enoxybenzene;Benzene, 1-(bromomethyl)-4-(2-propenyloxy)-;SCHEMBL5098606;DTXSID80464404;FEUUZYHKKUIYRW-UHFFFAOYSA-N;FT-0750525;EN300-4982843;A1-05153;1-(BROMOMETHYL)-4-(PROP-2-EN-1-YLOXY)BENZENE

Suppliers and Price of 4-Allyloxybenzyl bromide

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 1 raw suppliers

Chemical Property of 4-Allyloxybenzyl bromide

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:225.99933
Heavy Atom Count:12
Complexity:128

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCOC1=CC=C(C=C1)CBr

Technology Process of 4-Allyloxybenzyl bromide

There total 5 articles about 4-Allyloxybenzyl bromide 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: 90.0%

: 3256-45-9
4-allyloxybenzyl alcohol

: 143116-30-7
1-(allyloxy)-4-(bromomethyl)benzene

Guidance literature:: With phosphorus tribromide; In diethyl ether; at 20 ℃; for 1h;
DOI:10.1002/anie.201710089

Reference yield:

: 623-05-2
(4-hydroxyphenyl)methanol

: 143116-30-7
1-(allyloxy)-4-(bromomethyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃

2: PBr₃

With phosphorus tribromide; potassium carbonate;
DOI:10.1021/jo010077l