Ethyl 5-(trifluoromethyl)-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. The presence of a trifluoromethyl group (-CF3) significantly enhances its lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry. The ethyl ester functional group contributes to its reactivity and solubility properties, allowing for potential applications in organic synthesis and pharmaceuticals. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its unique structure may impart specific electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, the trifluoromethyl group can enhance the compound's metabolic stability and alter its interaction with biological targets, which is valuable in drug design. Overall, ethyl 5-(trifluoromethyl)-1,2,4-oxadiazole-3-carboxylate is a versatile compound with potential applications in various fields, including agrochemicals and pharmaceuticals.

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

914773-13-0: Ethyl 5-(trifluoromethyl)-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. The presence of a trifluoromethyl group (-CF3) significantly enhances its lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry. The ethyl ester functional group contributes to its reactivity and solubility properties, allowing for potential applications in organic synthesis and pharmaceuticals. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its unique structure may impart specific electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, the trifluoromethyl group can enhance the compound's metabolic stability and alter its interaction with biological targets, which is valuable in drug design. Overall, ethyl 5-(trifluoromethyl)-1,2,4-oxadiazole-3-carboxylate is a versatile compound with potential applications in various fields, including agrochemicals and pharmaceuticals.

CAS 914773-13-0

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

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

Ref: IN-DA00IGQ3

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

Ref: 10-F224528