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CAS 93514-82-0

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Ethyl 5,7-dichloro-4-hydroxy-3-quinolinecarboxylate

Description:
Ethyl 5,7-dichloro-4-hydroxy-3-quinolinecarboxylate is a chemical compound characterized by its quinoline structure, which features a fused bicyclic aromatic system. This compound contains two chlorine substituents at the 5 and 7 positions, contributing to its reactivity and potential biological activity. The presence of a hydroxy group at the 4 position enhances its solubility in polar solvents and may influence its interaction with biological targets. The ethyl ester functional group at the carboxylate position suggests that it can undergo hydrolysis to release the corresponding carboxylic acid, which may have implications for its pharmacological properties. This compound is of interest in medicinal chemistry, particularly for its potential applications in developing antimicrobial or anticancer agents. Its molecular structure allows for various synthetic modifications, which can be explored to enhance its efficacy or reduce toxicity. As with many halogenated compounds, it is essential to consider environmental and safety aspects during handling and disposal.
Formula:C12H9Cl2NO3
InChI:InChI=1/C12H9Cl2NO3/c1-2-18-12(17)7-5-15-9-4-6(13)3-8(14)10(9)11(7)16/h3-5H,2H2,1H3,(H,15,16)
InChI key:InChIKey=ZGUZVDPXYSBFGE-UHFFFAOYSA-N
SMILES:OC=1C2=C(N=CC1C(OCC)=O)C=C(Cl)C=C2Cl
Synonyms:
  • 3-Quinolinecarboxylic Acid, 5,7-Dichloro-1,4-Dihydro-4-Oxo-, Ethyl Ester
  • 3-Quinolinecarboxylic Acid, 5,7-Dichloro-4-Hydroxy-, Ethyl Ester
  • Ethyl 5,7-dichloro-4-hydroxy-3-quinolinecarboxylate
  • Ethyl 5,7-dichloro-4-hydroxyquinoline-3-carboxylate
  • Ethyl 5,7-dichloro-4-oxo-1,4-dihydroquinoline-3-carboxylate
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