1-(Bromomethyl)-4-butylcyclohexane

Base Information Edit

Chemical Name:1-(Bromomethyl)-4-butylcyclohexane
CAS No.:71458-13-4
Molecular Formula:C11H21Br
Molecular Weight:233.192
Hs Code.:
DSSTox Substance ID:DTXSID901277324
Mol file:71458-13-4.mol

Synonyms:1-(bromomethyl)-4-butylcyclohexane;SCHEMBL7751705;SCHEMBL7913395;DTXSID901277324;AKOS008967260;71458-13-4;trans-1-(Bromomethyl)-4-butylcyclohexane;EN300-675190;192123-09-4

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

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(Bromomethyl)-4-butylcyclohexane Edit

Chemical Property:

XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:4
Exact Mass:232.08266
Heavy Atom Count:12
Complexity:104

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCC1CCC(CC1)CBr

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

There total 7 articles about 1-(Bromomethyl)-4-butylcyclohexane 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: 76.0%

: 71458-07-6
trans-4-n-Butylcyclohexylmethanol

: 71458-13-4
1-Bromomethyl-4-butyl-cyclohexane

Guidance literature:: With sulfuric acid; hydrogen bromide;

Reference yield:

: 38289-28-0
trans-4-butylcyclohexanecarboxylic acid

: 71458-13-4
1-Bromomethyl-4-butyl-cyclohexane

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / SOCl₂

2: 91 percent / LiAlH₄ / diethyl ether

3: 76 percent / HBr, aq/H₂SO₄

With lithium aluminium tetrahydride; thionyl chloride; sulfuric acid; hydrogen bromide; In diethyl ether;

Reference yield:

: 67589-89-3,146606-05-5
trans-4-n-butylcyclohexane-carboxylic acid chloride

: 71458-13-4
1-Bromomethyl-4-butyl-cyclohexane

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / LiAlH₄ / diethyl ether

2: 76 percent / HBr, aq/H₂SO₄

With lithium aluminium tetrahydride; sulfuric acid; hydrogen bromide; In diethyl ether;