4-Fluoro-N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]benzamide is a chemical compound characterized by its unique structural features, which include a benzamide moiety and a thiadiazole ring. The presence of a fluorine atom at the para position of the benzene ring enhances its lipophilicity and may influence its biological activity. The thiadiazole ring contributes to the compound's potential pharmacological properties, as thiadiazoles are often associated with various biological activities, including antimicrobial and anti-inflammatory effects. The ketone group in the 2-oxopropyl side chain can participate in hydrogen bonding, which may affect the compound's solubility and reactivity. This compound is of interest in medicinal chemistry and drug development due to its potential therapeutic applications. Its specific interactions with biological targets would depend on its conformation and the presence of functional groups that facilitate binding. As with many synthetic compounds, safety and handling precautions should be observed, and its environmental impact should be assessed in accordance with regulatory guidelines.

4-fluoro-N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]benzamide

690991-52-7: 4-Fluoro-N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]benzamide is a chemical compound characterized by its unique structural features, which include a benzamide moiety and a thiadiazole ring. The presence of a fluorine atom at the para position of the benzene ring enhances its lipophilicity and may influence its biological activity. The thiadiazole ring contributes to the compound's potential pharmacological properties, as thiadiazoles are often associated with various biological activities, including antimicrobial and anti-inflammatory effects. The ketone group in the 2-oxopropyl side chain can participate in hydrogen bonding, which may affect the compound's solubility and reactivity. This compound is of interest in medicinal chemistry and drug development due to its potential therapeutic applications. Its specific interactions with biological targets would depend on its conformation and the presence of functional groups that facilitate binding. As with many synthetic compounds, safety and handling precautions should be observed, and its environmental impact should be assessed in accordance with regulatory guidelines.

CAS 690991-52-7

4-fluoro-N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]benzamide

4-fluoro-N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]benzamide

Ref: 10-F315449