Ethyl 3-(o-hydroxybenzoyl)propionate

Base Information

Chemical Name:Ethyl 3-(o-hydroxybenzoyl)propionate
CAS No.:39496-84-9
Molecular Formula:C₁₂H₁₄O₄
Molecular Weight:222.241
Hs Code.:
DSSTox Substance ID:DTXSID301286967

Synonyms:Ethyl 3-(o-hydroxybenzoyl)propionate;SCHEMBL9348474;LHJKRORWBXZUOC-UHFFFAOYSA-N;DTXSID301286967;39496-84-9;Ethyl 2-hydroxy-I(3)-oxobenzenebutanoate

Suppliers and Price of Ethyl 3-(o-hydroxybenzoyl)propionate

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Ethyl 3-(o-hydroxybenzoyl)propionate

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:222.08920892
Heavy Atom Count:16
Complexity:249

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)CCC(=O)C1=CC=CC=C1O

Technology Process of Ethyl 3-(o-hydroxybenzoyl)propionate

There total 4 articles about Ethyl 3-(o-hydroxybenzoyl)propionate 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:

: 7664-93-9
sulfuric acid

: 39560-34-4
3-(2-hydroxybenzoyl)propionic acid

: 39496-84-9
4-(2-hydroxy-phenyl)-4-oxo-butyric acid ethyl ester

Guidance literature:: In ethanol;

Reference yield:

: 39560-34-4
3-(2-hydroxybenzoyl)propionic acid

: 39496-84-9
4-(2-hydroxy-phenyl)-4-oxo-butyric acid ethyl ester

Guidance literature:: With ethanol; mineral acid;

Reference yield:

: 108-95-2,27073-41-2
phenol

: 39496-84-9
4-(2-hydroxy-phenyl)-4-oxo-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aluminium chloride; 1.1.2.2-tetrachloro-ethane / 120 - 140 °C

2: ethanol; mineral acid

With aluminium trichloride; ethanol; mineral acid; 1,1,2,2-tetrachloroethane;