2-Propenoic acid, 3-phenyl-, 4-acetylphenyl ester

Base Information

Chemical Name:2-Propenoic acid, 3-phenyl-, 4-acetylphenyl ester
CAS No.:84796-16-7
Molecular Formula:C17H14O3
Molecular Weight:266.296
Hs Code.:
DSSTox Substance ID:DTXSID20355281

Synonyms:2-Propenoic acid, 3-phenyl-, 4-acetylphenyl ester;84796-16-7;DTXSID20355281

Suppliers and Price of 2-Propenoic acid, 3-phenyl-, 4-acetylphenyl ester

Supply Marketing:

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

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Chemical Property of 2-Propenoic acid, 3-phenyl-, 4-acetylphenyl ester

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:266.094294304
Heavy Atom Count:20
Complexity:358

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CC=C(C=C1)OC(=O)C=CC2=CC=CC=C2

Technology Process of 2-Propenoic acid, 3-phenyl-, 4-acetylphenyl ester

There total 3 articles about 2-Propenoic acid, 3-phenyl-, 4-acetylphenyl ester 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%

: 102-92-1,17082-09-6
Cinnamoyl chloride

: 99-93-4
4-Hydroxyacetophenone

: 84796-16-7
(E)-4-acetophenyl cinnamate

Guidance literature:: With pyridine; In benzene; for 1h; Heating;

Reference yield: 61.0%

: 140-10-3
(E)-3-phenylacrylic acid

: 99-93-4
4-Hydroxyacetophenone

: 84796-16-7
(E)-4-acetophenyl cinnamate

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In acetonitrile; at 40 - 45 ℃; for 0.75h;
DOI:10.1016/j.bmc.2018.04.007