(Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate

Base Information

Chemical Name:(Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate
CAS No.:1416979-69-5
Molecular Formula:C₁₉H₁₃BrCl₃F₃O₂
Molecular Weight:516.569
Hs Code.:

Synonyms:(Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate

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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 (Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate

Chemical Property:

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Technology Process of (Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate

There total 1 articles about (Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate 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:

: 1416979-69-5
(Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate

Guidance literature:

Reference yield:

: 1416979-69-5
(Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate

: 1416979-93-5
(Z)-2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoic acid

Guidance literature:: With trimethylsilyl iodide; In dichloromethane; ethyl acetate; acetonitrile;

Reference yield:

: 1416979-69-5
(Z)-ethyl 2-bromo-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzoate

: 1416977-61-1
(Z)-2-Bromo-N-(2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: trimethylsilyl iodide / dichloromethane; acetonitrile; ethyl acetate

2: 1,1'-carbonyldiimidazole / tetrahydrofuran; diethyl ether

With trimethylsilyl iodide; 1,1'-carbonyldiimidazole; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate; acetonitrile;