5-(3-Chloropropyl)-3-phenyl-1,2,4-oxadiazole is a chemical compound characterized by its oxadiazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms and three carbon atoms. The presence of a phenyl group and a 3-chloropropyl substituent contributes to its unique properties. This compound typically exhibits moderate to high lipophilicity due to the aromatic phenyl group, which can influence its solubility in organic solvents. The chloropropyl group may impart additional reactivity, making it a potential candidate for further chemical modifications or applications in medicinal chemistry. Oxadiazoles are known for their diverse biological activities, including antimicrobial and anti-inflammatory properties, which may be relevant for pharmaceutical research. The compound's stability, reactivity, and potential applications can vary based on its specific molecular interactions and the presence of functional groups. Overall, 5-(3-chloropropyl)-3-phenyl-1,2,4-oxadiazole represents a versatile structure in organic synthesis and drug development.

5-(3-chloropropyl)-3-phenyl-1,2,4-oxadiazole

91066-23-8: 5-(3-Chloropropyl)-3-phenyl-1,2,4-oxadiazole is a chemical compound characterized by its oxadiazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms and three carbon atoms. The presence of a phenyl group and a 3-chloropropyl substituent contributes to its unique properties. This compound typically exhibits moderate to high lipophilicity due to the aromatic phenyl group, which can influence its solubility in organic solvents. The chloropropyl group may impart additional reactivity, making it a potential candidate for further chemical modifications or applications in medicinal chemistry. Oxadiazoles are known for their diverse biological activities, including antimicrobial and anti-inflammatory properties, which may be relevant for pharmaceutical research. The compound's stability, reactivity, and potential applications can vary based on its specific molecular interactions and the presence of functional groups. Overall, 5-(3-chloropropyl)-3-phenyl-1,2,4-oxadiazole represents a versatile structure in organic synthesis and drug development.

CAS 91066-23-8

5-(3-chloropropyl)-3-phenyl-1,2,4-oxadiazole

5-(3-Chloropropyl)-3-phenyl-1,2,4-oxadiazole

Ref: 3D-RDA06623