Ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate 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 an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the 4-methoxyphenyl group enhances its aromatic character and may influence its biological activity and interaction with other molecules. Typically, compounds like this can exhibit a range of properties, including potential pharmaceutical applications due to their ability to interact with biological targets. The oxadiazole moiety is often associated with various biological activities, including antimicrobial and anti-inflammatory effects. Additionally, the compound's structure suggests it may participate in hydrogen bonding and π-π stacking interactions, which are important in drug design and molecular recognition. Overall, ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate represents a class of compounds with diverse applications in medicinal chemistry and materials science.

ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate

151098-14-5: Ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate 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 an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the 4-methoxyphenyl group enhances its aromatic character and may influence its biological activity and interaction with other molecules. Typically, compounds like this can exhibit a range of properties, including potential pharmaceutical applications due to their ability to interact with biological targets. The oxadiazole moiety is often associated with various biological activities, including antimicrobial and anti-inflammatory effects. Additionally, the compound's structure suggests it may participate in hydrogen bonding and π-π stacking interactions, which are important in drug design and molecular recognition. Overall, ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate represents a class of compounds with diverse applications in medicinal chemistry and materials science.

Ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate

Ethyl 5-(4-methoxyphenyl)-[1,2,4]oxadiazole-3-carboxylate

CAS 151098-14-5

ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate

Ethyl 5-(4-methoxyphenyl)-1,2,4-oxadiazole-3-carboxylate

Ref: IN-DA001N33

Ethyl 5-(4-methoxyphenyl)-[1,2,4]oxadiazole-3-carboxylate

Ref: 54-OR346024