(E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime

Base Information

Chemical Name:(E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime
CAS No.:1311378-41-2
Molecular Formula:C₂₁H₂₀F₃NO₂
Molecular Weight:375.391
Hs Code.:

Synonyms:(E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime

Suppliers and Price of (E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime

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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 (E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime

Chemical Property:

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Technology Process of (E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime

There total 1 articles about (E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime 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:

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 1388625-06-6
C₁₃H₁₇NO₂

: 1311378-41-2
(E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime

Guidance literature:: In tetrahydrofuran; at 65 ℃; for 2h;
DOI:10.1055/s-0031-1290819

Reference yield:

: 1311378-41-2
(E)-4-(trifluoromethyl)benzaldehyde O-[1-(4-methoxyphenyl)hex-1-yn-3-yl]oxime

: 1311378-55-8
(E)-3-butylidene-4-(4-methoxyphenyl)-2-(4-(trifluoromethyl)phenyl)-2,3-dihydroazete 1-oxide

: (Z)-3-butylidene-4-(4-methoxyphenyl)-2-(4-(trifluoromethyl)phenyl)-2,3-dihydroazete 1-oxide

Guidance literature:: With [CuCl(cod)]2; In acetonitrile; at 100 ℃; for 24h; optical yield given as %de; regioselective reaction; Inert atmosphere;
DOI:10.1021/ol2012583