5-(Chloromethyl)-3-(3,4-dimethoxyphenyl)-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. This compound features a chloromethyl group, which enhances its reactivity and potential for further chemical modifications. The presence of the 3,4-dimethoxyphenyl group contributes to its aromatic character and may influence its solubility and electronic properties. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis due to their unique structural features. The oxadiazole moiety is often associated with biological activity, making such compounds of interest in medicinal chemistry. Additionally, the chloromethyl group can serve as a site for nucleophilic substitution reactions, allowing for the introduction of various functional groups. Overall, this compound exemplifies the diverse chemistry of heterocycles and their utility in various chemical applications.

5-(chloromethyl)-3-(3,4-dimethoxyphenyl)-1,2,4-oxadiazole

91066-47-6: 5-(Chloromethyl)-3-(3,4-dimethoxyphenyl)-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. This compound features a chloromethyl group, which enhances its reactivity and potential for further chemical modifications. The presence of the 3,4-dimethoxyphenyl group contributes to its aromatic character and may influence its solubility and electronic properties. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis due to their unique structural features. The oxadiazole moiety is often associated with biological activity, making such compounds of interest in medicinal chemistry. Additionally, the chloromethyl group can serve as a site for nucleophilic substitution reactions, allowing for the introduction of various functional groups. Overall, this compound exemplifies the diverse chemistry of heterocycles and their utility in various chemical applications.

CAS 91066-47-6

5-(chloromethyl)-3-(3,4-dimethoxyphenyl)-1,2,4-oxadiazole

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

Ref: IN-DA006F06

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

Ref: 54-OR300569

5-Chloromethyl-3-(3,4-dimethoxyphenyl)-[1,2,4]oxadiazole

Ref: 10-F047434