5-(4-Fluorophenyl)-1,3,4-oxadiazol-2(3H)-one is a heterocyclic compound characterized by the presence of an oxadiazole ring, which is a five-membered ring containing two nitrogen atoms and three carbon atoms, with an oxygen atom incorporated into the structure. The compound features a 4-fluorophenyl group, indicating the presence of a fluorine atom on a phenyl ring, which can influence its electronic properties and reactivity. This compound is known for its potential biological activity, making it of interest in medicinal chemistry and drug development. Its structure suggests it may exhibit properties such as antimicrobial, anti-inflammatory, or anticancer activities, although specific biological effects would depend on further empirical studies. The presence of the oxadiazole moiety often contributes to the compound's stability and solubility characteristics. Additionally, the fluorine substituent can enhance lipophilicity and metabolic stability, which are important factors in pharmacokinetics. Overall, this compound represents a class of substances that may have significant applications in pharmaceuticals and agrochemicals.

5-(4-FLUOROPHENYL)-1,3,4-OXADIAZOL-2(3H)-ONE

121649-18-1: 5-(4-Fluorophenyl)-1,3,4-oxadiazol-2(3H)-one is a heterocyclic compound characterized by the presence of an oxadiazole ring, which is a five-membered ring containing two nitrogen atoms and three carbon atoms, with an oxygen atom incorporated into the structure. The compound features a 4-fluorophenyl group, indicating the presence of a fluorine atom on a phenyl ring, which can influence its electronic properties and reactivity. This compound is known for its potential biological activity, making it of interest in medicinal chemistry and drug development. Its structure suggests it may exhibit properties such as antimicrobial, anti-inflammatory, or anticancer activities, although specific biological effects would depend on further empirical studies. The presence of the oxadiazole moiety often contributes to the compound's stability and solubility characteristics. Additionally, the fluorine substituent can enhance lipophilicity and metabolic stability, which are important factors in pharmacokinetics. Overall, this compound represents a class of substances that may have significant applications in pharmaceuticals and agrochemicals.

5-(4-Fluorophenyl)-3H-1,3,4-oxadiazol-2-one

<p>5-(4-Fluorophenyl)-1,3,4-oxadiazol-2(3H)-one</p>

CAS 121649-18-1

5-(4-FLUOROPHENYL)-1,3,4-OXADIAZOL-2(3H)-ONE

5-(4-Fluorophenyl)-3H-1,3,4-oxadiazol-2-one

Ref: IN-DA0015I1

5-(4-Fluorophenyl)-1,3,4-oxadiazol-2(3H)-one

Ref: 54-PC200516