Methyl 2-amino-4-(4-methylphenyl)thiophene-3-carboxylate, identified by its CAS number 350997-08-9, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and a carboxylate ester group (-COOCH3), contributing to its reactivity and potential applications in medicinal chemistry. The presence of the 4-methylphenyl substituent enhances its lipophilicity and may influence its biological activity. Methyl 2-amino-4-(4-methylphenyl)thiophene-3-carboxylate is likely to exhibit properties typical of thiophene derivatives, such as fluorescence and the ability to participate in various chemical reactions, including electrophilic substitutions. Its structural features suggest potential utility in the development of pharmaceuticals or agrochemicals, particularly in the synthesis of compounds targeting specific biological pathways. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups.

methyl 2-amino-4-(4-methylphenyl)thiophene-3-carboxylate

350997-08-9: Methyl 2-amino-4-(4-methylphenyl)thiophene-3-carboxylate, identified by its CAS number 350997-08-9, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and a carboxylate ester group (-COOCH3), contributing to its reactivity and potential applications in medicinal chemistry. The presence of the 4-methylphenyl substituent enhances its lipophilicity and may influence its biological activity. Methyl 2-amino-4-(4-methylphenyl)thiophene-3-carboxylate is likely to exhibit properties typical of thiophene derivatives, such as fluorescence and the ability to participate in various chemical reactions, including electrophilic substitutions. Its structural features suggest potential utility in the development of pharmaceuticals or agrochemicals, particularly in the synthesis of compounds targeting specific biological pathways. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups.

CAS 350997-08-9

methyl 2-amino-4-(4-methylphenyl)thiophene-3-carboxylate

2-Amino-4-p-tolylthiophene-3-carboxylic acidmethyl ester

Ref: 10-F014044