5-(Chloromethyl)-3-(furan-2-yl)-1,2,4-oxadiazole 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. The compound features a chloromethyl group, which enhances its reactivity and potential for further chemical modifications. The furan moiety contributes to its aromatic character and may influence its electronic properties and reactivity. This compound is typically of interest in medicinal chemistry and materials science due to its potential biological activities and applications in organic synthesis. Its structure suggests that it may exhibit properties such as fluorescence or antimicrobial activity, although specific biological activities would need to be evaluated through experimental studies. Additionally, the presence of the chloromethyl group may facilitate nucleophilic substitution reactions, making it a versatile intermediate in the synthesis of more complex molecules. Overall, 5-(chloromethyl)-3-(furan-2-yl)-1,2,4-oxadiazole is a compound with significant potential for various applications in chemical research.

5-(chloromethyl)-3-(furan-2-yl)-1,2,4-oxadiazole

501653-22-1: 5-(Chloromethyl)-3-(furan-2-yl)-1,2,4-oxadiazole 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. The compound features a chloromethyl group, which enhances its reactivity and potential for further chemical modifications. The furan moiety contributes to its aromatic character and may influence its electronic properties and reactivity. This compound is typically of interest in medicinal chemistry and materials science due to its potential biological activities and applications in organic synthesis. Its structure suggests that it may exhibit properties such as fluorescence or antimicrobial activity, although specific biological activities would need to be evaluated through experimental studies. Additionally, the presence of the chloromethyl group may facilitate nucleophilic substitution reactions, making it a versatile intermediate in the synthesis of more complex molecules. Overall, 5-(chloromethyl)-3-(furan-2-yl)-1,2,4-oxadiazole is a compound with significant potential for various applications in chemical research.

CAS 501653-22-1

5-(chloromethyl)-3-(furan-2-yl)-1,2,4-oxadiazole

5-(Chloromethyl)-3-(2-furyl)-1,2,4-oxadiazole

Ref: 10-F069841

5-(Chloromethyl)-3-(2-furyl)-1,2,4-oxadiazole

Ref: 3D-BVA65322