Benzene, (2-cyclohexyl-1-propenyl)-, (E)-

Base Information

Chemical Name:Benzene, (2-cyclohexyl-1-propenyl)-, (E)-
CAS No.:104531-92-2
Molecular Formula:C15H20
Molecular Weight:200.324
Hs Code.:
Mol file:104531-92-2.mol

Synonyms:

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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 Benzene, (2-cyclohexyl-1-propenyl)-, (E)-

Chemical Property:

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MSDS Files:: SDS file from LookChem

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Technology Process of Benzene, (2-cyclohexyl-1-propenyl)-, (E)-

There total 8 articles about Benzene, (2-cyclohexyl-1-propenyl)-, (E)- 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: 88.0%

: 673-32-5
1-Phenylprop-1-yne

: 1-cyclohexyl-2,4,6-triphenylpyridin-1-ium tetrafluoroborate salt

: 104531-92-2
(E)-(2-cyclohexylprop-1-en-1-yl)benzene

Guidance literature:: 1-cyclohexyl-2,4,6-triphenylpyridin-1-ium tetrafluoroborate salt; With nickel(II) bromide dimethoxyethane; potassium carbonate; 4,4'-di-tert-butyl-2,2'-bipyridine; at 20 ℃; Schlenk technique; Sealed tube; Inert atmosphere;

1-Phenylprop-1-yne; With 1,1,3,3-Tetramethyldisiloxane; In N,N-dimethyl acetamide; at 20 ℃; regioselective reaction; Schlenk technique; Sealed tube; Inert atmosphere;
DOI:10.1039/c9cc05385a

Reference yield: 81.0%

: 673-32-5
1-Phenylprop-1-yne

: 626-62-0
Cyclohexyl iodide

: 104531-92-2
(E)-(2-cyclohexylprop-1-en-1-yl)benzene

Guidance literature:: 1-Phenylprop-1-yne; Cyclohexyl iodide; With nickel(II) bromide dimethoxyethane; potassium carbonate; 4,4'-di-tert-butyl-2,2'-bipyridine; In N,N-dimethyl acetamide; for 0.0833333h; Schlenk technique; Inert atmosphere;

With diethoxymethylsilane; In N,N-dimethyl acetamide; at 30 ℃; for 10h; Reagent/catalyst; Solvent; stereoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1039/c8cc01577e

Reference yield: 75.0%

: 673-32-5
1-Phenylprop-1-yne

: 126812-30-4
1,3-dioxoisoindolin-2-yl cyclohexanecarboxylate

: 104531-92-2
(E)-(2-cyclohexylprop-1-en-1-yl)benzene

Guidance literature:: With 1,1,3,3-Tetramethyldisiloxane; nickel(II) chloride2-methoxyethyl ether; calcium acetate; 4,4'-di-tert-butyl-2,2'-bipyridine; In N,N-dimethyl acetamide; at 40 ℃; for 4h; regioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1016/j.tet.2018.10.037