Benzene, 1-(chloromethyl)-4-heptyl-

Base Information

Chemical Name:Benzene, 1-(chloromethyl)-4-heptyl-
CAS No.:58999-68-1
Molecular Formula:C14H21Cl
Molecular Weight:224.774
Hs Code.:
DSSTox Substance ID:DTXSID00482564
Wikidata:Q82319021

Synonyms:Benzene, 1-(chloromethyl)-4-heptyl-;58999-68-1;DTXSID00482564

Suppliers and Price of Benzene, 1-(chloromethyl)-4-heptyl-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Benzene, 1-(chloromethyl)-4-heptyl-

Chemical Property:

XLogP3:6.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:7
Exact Mass:224.1331784
Heavy Atom Count:15
Complexity:136

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC1=CC=C(C=C1)CCl

Technology Process of Benzene, 1-(chloromethyl)-4-heptyl-

There total 3 articles about Benzene, 1-(chloromethyl)-4-heptyl- 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: 87.0%

: 861906-61-8
4-heptylbenzyl diphenylphosphinate

: 58999-68-1
4-heptylbenzyl chloride

Guidance literature:: With titanium tetrachloride; allyl-trimethyl-silane; In chloroform; at 20 ℃; for 7h;
DOI:10.1246/cl.2005.756

Reference yield:

: 171627-60-4
4-heptylbenzyl alcohol

: 58999-68-1
4-heptylbenzyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine

2: 87 percent / allyltrimethylsilane; TiCl₄ / CHCl₃ / 7 h / 20 °C

With titanium tetrachloride; triethylamine; allyl-trimethyl-silane; In chloroform;
DOI:10.1246/cl.2005.756