Ethyl 3-(2-chloro-6-fluorophenyl)-2-[1-(6-fluoro-2-pyridinyl)-1H-pyrazol-5-yl]propanoate, identified by its CAS number 477709-64-1, is a synthetic organic compound characterized by its complex molecular structure, which includes an ethyl ester functional group, a chlorinated aromatic ring, and a fluorinated pyridine moiety. This compound is typically used in pharmaceutical research and development, particularly in the context of drug discovery, due to its potential biological activity. The presence of halogen substituents, such as chlorine and fluorine, often enhances the lipophilicity and metabolic stability of the molecule, which can influence its pharmacokinetic properties. Additionally, the pyrazole ring contributes to its potential as a bioactive agent, as pyrazoles are known for their diverse biological activities, including anti-inflammatory and analgesic effects. Overall, the unique combination of functional groups in this compound suggests it may interact with specific biological targets, making it a subject of interest in medicinal chemistry.

ETHYL 3-(2-CHLORO-6-FLUOROPHENYL)-2-[1-(6-FLUORO-2-PYRIDINYL)-1H-PYRAZOL-5-YL]PROPANOATE

477709-64-1: Ethyl 3-(2-chloro-6-fluorophenyl)-2-[1-(6-fluoro-2-pyridinyl)-1H-pyrazol-5-yl]propanoate, identified by its CAS number 477709-64-1, is a synthetic organic compound characterized by its complex molecular structure, which includes an ethyl ester functional group, a chlorinated aromatic ring, and a fluorinated pyridine moiety. This compound is typically used in pharmaceutical research and development, particularly in the context of drug discovery, due to its potential biological activity. The presence of halogen substituents, such as chlorine and fluorine, often enhances the lipophilicity and metabolic stability of the molecule, which can influence its pharmacokinetic properties. Additionally, the pyrazole ring contributes to its potential as a bioactive agent, as pyrazoles are known for their diverse biological activities, including anti-inflammatory and analgesic effects. Overall, the unique combination of functional groups in this compound suggests it may interact with specific biological targets, making it a subject of interest in medicinal chemistry.

CAS 477709-64-1

ETHYL 3-(2-CHLORO-6-FLUOROPHENYL)-2-[1-(6-FLUORO-2-PYRIDINYL)-1H-PYRAZOL-5-YL]PROPANOATE