1-(Bromomethyl)-4-octylbenzene

Base Information

Chemical Name:1-(Bromomethyl)-4-octylbenzene
CAS No.:88255-11-2
Molecular Formula:C15H23Br
Molecular Weight:283.252
Hs Code.:
DSSTox Substance ID:DTXSID70548267
Nikkaji Number:J1.830.858D
Wikidata:Q82426910
Mol file:88255-11-2.mol

Synonyms:88255-11-2;1-(BROMOMETHYL)-4-OCTYLBENZENE;4-Octylbenzyl bromide;1-Bromomethyl-4-octylbenzene;Benzene, 1-(bromomethyl)-4-octyl-;4-n-octylbenzyl bromide;SCHEMBL177117;1-Bromomethyl-4-octyl-benzene;DTXSID70548267;QPRYBIJQSRFLBQ-UHFFFAOYSA-N;AC8311;MFCD20485145;SY262751;A900876;A1-03791

Suppliers and Price of 1-(Bromomethyl)-4-octylbenzene

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

AK Scientific
1-(Bromomethyl)-4-octylbenzene
1g
$ 1342.00

A1 Biochem Labs
1-Bromomethyl-4-octyl-benzene 95%
1 g
$ 750.00

Total 9 raw suppliers

Chemical Property of 1-(Bromomethyl)-4-octylbenzene

Chemical Property:

PSA：0.00000
LogP:5.48450
XLogP3:6.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:8
Exact Mass:282.09831
Heavy Atom Count:16
Complexity:148

Purity/Quality:

97% ^*data from raw suppliers

1-(Bromomethyl)-4-octylbenzene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCC1=CC=C(C=C1)CBr

Technology Process of 1-(Bromomethyl)-4-octylbenzene

There total 7 articles about 1-(Bromomethyl)-4-octylbenzene 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: 79.0%

: 40016-25-9
4-n-octylbenzenemethanol

: 88255-11-2
p-(n-octyl)benzyl bromide

Guidance literature:: With phosphorus tribromide; In diethyl ether; at 90 ℃; for 2h;

Reference yield: 28.0%

: 623-24-5
1,4-bis(bromomethyl)benzene

: 13125-66-1
n-heptylmagnesium bromide

: 88255-11-2
p-(n-octyl)benzyl bromide

Guidance literature:: With copper(I) bromide dimethylsulfide complex; In diethyl ether; at 0 ℃; for 18h;
DOI:10.1016/S0040-4039(01)02024-X

Reference yield:

: 54256-51-8
4-octyl-benzoic acid methyl ester

: 88255-11-2
p-(n-octyl)benzyl bromide

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄

2: phosphorus tribromide

With lithium aluminium tetrahydride; phosphorus tribromide;
DOI:10.1246/bcsj.64.2714