Benzene, 1-propylhexyl

Base Information

Chemical Name:Benzene, 1-propylhexyl
CAS No.:65185-83-3
Molecular Formula:C₁₅H₂₄
Molecular Weight:204.356
Hs Code.:
DSSTox Substance ID:DTXSID101314205
Nikkaji Number:J2.684.094E

Synonyms:Benzene, 1-propylhexyl;4-Phenylnonane;(1-Propylhexyl)benzene;DTXSID101314205;65185-83-3

Suppliers and Price of Benzene, 1-propylhexyl

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Benzene, 1-propylhexyl

Chemical Property:

XLogP3:6.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:7
Exact Mass:204.187800766
Heavy Atom Count:15
Complexity:133

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCC(CCC)C1=CC=CC=C1

Technology Process of Benzene, 1-propylhexyl

There total 2 articles about Benzene, 1-propylhexyl 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: 98.0%

: 52708-14-2
4-bromononane

: 100-58-3
phenylmagnesium bromide

: 65185-83-3
(1-propylhexyl)benzene

Guidance literature:: With N,N,N,N,-tetramethylethylenediamine; cobalt(III) acetylacetonate; In tetrahydrofuran; at 0 ℃; for 0.666667h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/ol802362e

Reference yield: 10.0%

: 65950-00-7
(+/-)-1-propylhexyl 4-methylbenzenesulfonate

: 100-58-3
phenylmagnesium bromide

: 65185-83-3
(1-propylhexyl)benzene

Guidance literature:: With N,N,N,N,-tetramethylethylenediamine; cobalt(III) acetylacetonate; In tetrahydrofuran; at 0 ℃; for 0.666667h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/ol802362e