Ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate, identified by its CAS number 82546-91-6, is a chemical compound that belongs to the class of thiophene derivatives. This substance features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur, and is substituted with an amino group, ethyl groups, and a carboxylate ester. The presence of these functional groups contributes to its potential reactivity and solubility characteristics. Typically, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. The ethyl ester group can influence the compound's lipophilicity, affecting its absorption and distribution in biological systems. Additionally, the amino group may participate in hydrogen bonding, enhancing interactions with other molecules. Overall, ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate is a structurally complex compound that may have applications in medicinal chemistry and organic synthesis, although specific properties such as melting point, boiling point, and solubility would require empirical measurement or literature reference for precise values.

ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate

82546-91-6: Ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate, identified by its CAS number 82546-91-6, is a chemical compound that belongs to the class of thiophene derivatives. This substance features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur, and is substituted with an amino group, ethyl groups, and a carboxylate ester. The presence of these functional groups contributes to its potential reactivity and solubility characteristics. Typically, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. The ethyl ester group can influence the compound's lipophilicity, affecting its absorption and distribution in biological systems. Additionally, the amino group may participate in hydrogen bonding, enhancing interactions with other molecules. Overall, ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate is a structurally complex compound that may have applications in medicinal chemistry and organic synthesis, although specific properties such as melting point, boiling point, and solubility would require empirical measurement or literature reference for precise values.

CAS 82546-91-6

ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate

Ethyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate

Ref: 10-F239278