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Ethyl 3-(4-fluoroanilino)-3-oxopropanoate

Base Information
  • Chemical Name:Ethyl 3-(4-fluoroanilino)-3-oxopropanoate
  • CAS No.:104330-60-1
  • Molecular Formula:C11H12FNO3
  • Molecular Weight:225.22
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60589285
  • Nikkaji Number:J2.235.432I
  • Wikidata:Q82482552
  • Mol file:104330-60-1.mol
Ethyl 3-(4-fluoroanilino)-3-oxopropanoate

Synonyms:104330-60-1;Ethyl 3-(4-fluoroanilino)-3-oxopropanoate;Propanoic acid, 3-[(4-fluorophenyl)amino]-3-oxo-, ethyl ester;ETHYL 2-[(4-FLUOROPHENYL)CARBAMOYL]ACETATE;ethyl 3-[(4-fluorophenyl)amino]-3-oxopropanoate;Ethyl 3-((4-fluorophenyl)amino)-3-oxopropanoate;Cabozantinib Impurity 5;SCHEMBL680836;DTXSID60589285;DVIGICXZLWQQCP-UHFFFAOYSA-N;AKOS003496867;DB-114427;ethyl 3-(4-fluorophenylamino)-3-oxopropanoate

Suppliers and Price of Ethyl 3-(4-fluoroanilino)-3-oxopropanoate
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 2 raw suppliers
Chemical Property of Ethyl 3-(4-fluoroanilino)-3-oxopropanoate
Chemical Property:
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:225.08012141
  • Heavy Atom Count:16
  • Complexity:250
Purity/Quality:

99%+ *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC(=O)CC(=O)NC1=CC=C(C=C1)F
Technology Process of Ethyl 3-(4-fluoroanilino)-3-oxopropanoate

There total 5 articles about Ethyl 3-(4-fluoroanilino)-3-oxopropanoate 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:
Guidance literature:
With triethylamine; In acetone; at 0 - 20 ℃;
Guidance literature:
In 5,5-dimethyl-1,3-cyclohexadiene; at 130 ℃; for 1.5h; Solvent; Concentration;
Guidance literature:
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃; for 16h;
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