Ethyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and an ethyl ester functional group. This compound features a methoxyphenyl substituent, contributing to its aromatic properties and potentially influencing its reactivity and solubility. The presence of the amino group suggests that it may participate in hydrogen bonding, enhancing its interactions in biological systems or chemical reactions. The ethyl ester moiety indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid, which may have implications for its biological activity or pharmacological properties. Additionally, the methylthio group can affect the electronic properties of the thiophene ring, possibly enhancing its electron-donating capabilities. Overall, this compound may exhibit interesting chemical behavior and potential applications in medicinal chemistry or materials science, although specific biological or pharmacological activities would require further investigation.

ethyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate

350989-93-4: Ethyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and an ethyl ester functional group. This compound features a methoxyphenyl substituent, contributing to its aromatic properties and potentially influencing its reactivity and solubility. The presence of the amino group suggests that it may participate in hydrogen bonding, enhancing its interactions in biological systems or chemical reactions. The ethyl ester moiety indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid, which may have implications for its biological activity or pharmacological properties. Additionally, the methylthio group can affect the electronic properties of the thiophene ring, possibly enhancing its electron-donating capabilities. Overall, this compound may exhibit interesting chemical behavior and potential applications in medicinal chemistry or materials science, although specific biological or pharmacological activities would require further investigation.

CAS 350989-93-4

ethyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate

ethyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate

Ref: 10-F307173