Methyl 2-amino-4-(naphthalen-1-yl)thiophene-3-carboxylate is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and a naphthalene moiety. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of the naphthalene ring imparts aromatic characteristics, enhancing its stability and potential for π-π stacking interactions. The amino group can participate in hydrogen bonding, making the compound potentially useful in various biological applications. Additionally, the methyl ester group can influence the compound's lipophilicity, affecting its absorption and distribution in biological systems. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its unique structural features suggest potential applications in organic synthesis, materials science, and as a building block for more complex molecules. As with many organic compounds, its behavior in different solvents and under various conditions can significantly impact its reactivity and utility in chemical processes.

methyl 2-amino-4-(naphthalen-1-yl)thiophene-3-carboxylate

350997-17-0: Methyl 2-amino-4-(naphthalen-1-yl)thiophene-3-carboxylate is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and a naphthalene moiety. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of the naphthalene ring imparts aromatic characteristics, enhancing its stability and potential for π-π stacking interactions. The amino group can participate in hydrogen bonding, making the compound potentially useful in various biological applications. Additionally, the methyl ester group can influence the compound's lipophilicity, affecting its absorption and distribution in biological systems. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its unique structural features suggest potential applications in organic synthesis, materials science, and as a building block for more complex molecules. As with many organic compounds, its behavior in different solvents and under various conditions can significantly impact its reactivity and utility in chemical processes.

CAS 350997-17-0

methyl 2-amino-4-(naphthalen-1-yl)thiophene-3-carboxylate

2-Amino-4-naphthalen-1-yl-thiophene-3-carboxylic acid methyl ester

Ref: 10-F014067