(2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide

Base Information

Chemical Name:(2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide
CAS No.:1032285-69-0
Molecular Formula:C₂₈H₂₆FNO₂
Molecular Weight:427.518
Hs Code.:

Synonyms:(2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide

Suppliers and Price of (2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide

There total 1 articles about (2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide 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:

: 107-58-4,25267-41-8
N-tert-Butylacrylamide

: 153354-46-2
4-fluoro-4'-phenylethynylbenzophenone

: 1032285-72-5
(2E,4Z)-N-tert-butyl-4-(4-(4-fluorobenzoyl)phenyl)-5-phenylpenta-2,4-dienamide

: 1032285-69-0
(2E,4Z)-N-tert-butyl-5-(4-(4-fluorobenzoyl)phenyl)-4-phenylpenta-2,4-dienamide

Guidance literature:: With tri tert-butylphosphoniumtetrafluoroborate; [PdCl₂(cod)]; In N,N-dimethyl-formamide; at 100 ℃; for 24h; Title compound not separated from byproducts.;
DOI:10.1002/anie.200705558