Ethyl 5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate is a synthetic organic compound characterized by its quinoline structure, which features a fused bicyclic system. This compound contains two fluorine atoms at the 5 and 8 positions, contributing to its unique reactivity and potential biological activity. The presence of a carboxylate group enhances its solubility in polar solvents and may influence its interaction with biological targets. The ethyl ester functionality allows for further derivatization, making it a versatile intermediate in organic synthesis. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as quinoline derivatives are known for various pharmacological properties, including antimicrobial and anticancer activities. Its molecular structure suggests that it may exhibit interesting electronic properties due to the presence of electronegative fluorine atoms, which can affect the compound's reactivity and stability. Overall, ethyl 5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate represents a valuable compound for research in both synthetic and medicinal chemistry.

ethyl 5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

223690-43-5: Ethyl 5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate is a synthetic organic compound characterized by its quinoline structure, which features a fused bicyclic system. This compound contains two fluorine atoms at the 5 and 8 positions, contributing to its unique reactivity and potential biological activity. The presence of a carboxylate group enhances its solubility in polar solvents and may influence its interaction with biological targets. The ethyl ester functionality allows for further derivatization, making it a versatile intermediate in organic synthesis. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as quinoline derivatives are known for various pharmacological properties, including antimicrobial and anticancer activities. Its molecular structure suggests that it may exhibit interesting electronic properties due to the presence of electronegative fluorine atoms, which can affect the compound's reactivity and stability. Overall, ethyl 5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate represents a valuable compound for research in both synthetic and medicinal chemistry.

<p>Ethyl 5,8-difluoro-4-hydroxyquinoline-3-carboxylate</p>

CAS 223690-43-5

ethyl 5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

Ethyl 5,8-difluoro-4-hydroxyquinoline-3-carboxylate

Ref: 54-PC110075