CAS 99429-64-8: ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
Formula:C12H10ClNO3
InChI:InChI=1/C12H10ClNO3/c1-2-17-12(16)9-10(13)7-5-3-4-6-8(7)14-11(9)15/h3-6H,2H2,1H3,(H,14,15)
SMILES:CCOC(=O)c1c(c2ccccc2nc1O)Cl
Synonyms:- 3-Quinolinecarboxylic acid, 4-chloro-1,2-dihydro-2-oxo-, ethyl ester
- 3-Quinolinecarboxylic Acid, 4-Chloro-2-Hydroxy-, Ethyl Ester
- Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
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Found 6 products.
Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
CAS:Purity:97%Color and Shape:SolidMolecular weight:251.6699981689453Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
CAS:ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate inhibits NAD(P)H: quinone oxidoreductase 1.Formula:C12H10ClNO3Purity:99.19%Color and Shape:SolidMolecular weight:251.67Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
CAS:Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylatePurity:≥98%Molecular weight:251.67g/molEthyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
CAS:Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate is a regioselective hydrazine, which reacts with acid to form the corresponding ester. The reaction mechanism of this compound is based on the substitution of the chlorine atom by hydrazine, with the formation of an intermediate that reacts with water to produce a carboxylic acid. This reaction can be followed by infrared spectroscopy and NMR techniques. It has been used in the synthesis of several compounds, including phenyl acetate and 2,6-dimethoxybenzoic acid.Formula:C12H10ClNO3Purity:Min. 95%Molecular weight:251.67 g/molRef: 3D-FE135291
Discontinued productethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
CAS:Formula:C12H10ClNO3Purity:95%Color and Shape:SolidMolecular weight:251.6657Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
CAS:Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylatePurity:95%Molecular weight:251.67g/mol
