2-(4-Fluorophenyl)-2-(4-oxo-1-piperidyl)acetic acid, identified by its CAS number 886363-63-9, is a chemical compound characterized by its unique structural features. It contains a piperidine ring with a ketone functional group and a fluorophenyl moiety, which contributes to its potential biological activity. The presence of the fluorine atom can enhance lipophilicity and influence the compound's interaction with biological targets. This compound is likely to exhibit properties typical of carboxylic acids, such as acidity and the ability to form salts or esters. Its structural complexity suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. The compound's synthesis and characterization would involve standard organic chemistry techniques, including purification methods like crystallization or chromatography. Additionally, its stability, solubility, and reactivity would be important factors to consider for practical applications. Overall, 2-(4-fluorophenyl)-2-(4-oxo-1-piperidyl)acetic acid represents a compound of interest in the field of drug discovery and development.

2-(4-fluorophenyl)-2-(4-oxo-1-piperidyl)acetic acid

886363-63-9: 2-(4-Fluorophenyl)-2-(4-oxo-1-piperidyl)acetic acid, identified by its CAS number 886363-63-9, is a chemical compound characterized by its unique structural features. It contains a piperidine ring with a ketone functional group and a fluorophenyl moiety, which contributes to its potential biological activity. The presence of the fluorine atom can enhance lipophilicity and influence the compound's interaction with biological targets. This compound is likely to exhibit properties typical of carboxylic acids, such as acidity and the ability to form salts or esters. Its structural complexity suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. The compound's synthesis and characterization would involve standard organic chemistry techniques, including purification methods like crystallization or chromatography. Additionally, its stability, solubility, and reactivity would be important factors to consider for practical applications. Overall, 2-(4-fluorophenyl)-2-(4-oxo-1-piperidyl)acetic acid represents a compound of interest in the field of drug discovery and development.

CAS 886363-63-9

2-(4-fluorophenyl)-2-(4-oxo-1-piperidyl)acetic acid

(4-FLUORO-PHENYL)-(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID

Ref: IN-DA004A22

(4-Fluoro-phenyl)-(4-oxo-piperidin-1-yl)-acetic acid

Ref: 10-F040943