Ethyl (E)-3-(4-acetylphenyl)prop-2-enoate

Base Information

Chemical Name:Ethyl (E)-3-(4-acetylphenyl)prop-2-enoate
CAS No.:82989-26-2
Molecular Formula:C13H14O3
Molecular Weight:218.252
Hs Code.:
Nikkaji Number:J1.529.422A,J1.795.740F

Synonyms:Ethyl (E)-3-(4-acetylphenyl)prop-2-enoate;SCHEMBL5694716;(e)-ethyl 3-(4-acetylphenyl)acrylate;4-Acetylbenzeneacrylic acid ethyl ester;4-Acetyl-trans-cinnamic acid ethyl ester;ethyl (2E)-3-(4-acetylphenyl)-2-propenoate

Suppliers and Price of Ethyl (E)-3-(4-acetylphenyl)prop-2-enoate

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 1 raw suppliers

Chemical Property of Ethyl (E)-3-(4-acetylphenyl)prop-2-enoate

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:218.094294304
Heavy Atom Count:16
Complexity:273

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C=CC1=CC=C(C=C1)C(=O)C
Isomeric SMILES:CCOC(=O)/C=C/C1=CC=C(C=C1)C(=O)C

Technology Process of Ethyl (E)-3-(4-acetylphenyl)prop-2-enoate

There total 14 articles about Ethyl (E)-3-(4-acetylphenyl)prop-2-enoate 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: 99.0%

: 13329-40-3
4-Iodoacetophenone

: 140-88-5,9003-32-1
ethyl acrylate

: 82989-26-2
(E)-ethyl 3-(4-acetylphenyl)acrylate

Guidance literature:: With triethylamine; In acetonitrile; at 90 ℃; for 3h; Electrochemical reaction;
DOI:10.1039/c6nj02279k

Reference yield: 97.0%

: 99-90-1
para-bromoacetophenone

: 140-88-5,9003-32-1
ethyl acrylate

: 82989-26-2
(E)-ethyl 3-(4-acetylphenyl)acrylate

Guidance literature:: With PEG-OCOCH₂CH₂CO₂CH₂CH₂-supported 3-methyl-imidazolium*Cl; potassium carbonate; palladium diacetate; at 140 ℃; for 8h;
DOI:10.1055/s-2005-871566

Reference yield: 93.0%

: 623-73-4
diazoacetic acid ethyl ester

: 3457-45-2
p-formylacetophenone

: 82989-26-2
(E)-ethyl 3-(4-acetylphenyl)acrylate

Guidance literature:: With sodium disulfite; triphenyl-arsane; chloro[tetra(p-chlorophenyl)porphyrinato]iron(III); In water; toluene; at 80 ℃; for 8h;
DOI:10.1021/jo0709899