3-(Chloromethyl)-5-(3-thienyl)-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 thienyl group, derived from thiophene, contributes to the compound's aromatic character and may influence its electronic properties. This compound is of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activities and applications in organic synthesis. Its structure suggests possible interactions with biological targets, making it a candidate for further investigation in drug development. Additionally, the presence of both halogen and heteroatoms in its structure may impart unique properties, such as increased solubility or specific reactivity patterns. Overall, 3-(chloromethyl)-5-(3-thienyl)-1,2,4-oxadiazole represents a versatile scaffold for the exploration of new chemical entities.

3-(CHLOROMETHYL)-5-(3-THIENYL)-1,2,4-OXADIAZOLE

184970-24-9: 3-(Chloromethyl)-5-(3-thienyl)-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 thienyl group, derived from thiophene, contributes to the compound's aromatic character and may influence its electronic properties. This compound is of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activities and applications in organic synthesis. Its structure suggests possible interactions with biological targets, making it a candidate for further investigation in drug development. Additionally, the presence of both halogen and heteroatoms in its structure may impart unique properties, such as increased solubility or specific reactivity patterns. Overall, 3-(chloromethyl)-5-(3-thienyl)-1,2,4-oxadiazole represents a versatile scaffold for the exploration of new chemical entities.

CAS 184970-24-9

3-(CHLOROMETHYL)-5-(3-THIENYL)-1,2,4-OXADIAZOLE

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

Ref: IN-DA0074QZ

3-(Chloromethyl)-5-thien-3-yl-1,2,4-oxadiazole

Ref: 54-OR29094

3-(Chloromethyl)-5-thien-3-yl-1,2,4-oxadiazole

Ref: 3D-JHA97024