Methyl 2-amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxylate, with the CAS number 350997-34-1, is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group and a carboxylate ester, contributing to its potential reactivity and solubility properties. The presence of the methyl and phenyl substituents enhances its lipophilicity and may influence its biological activity. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The specific arrangement of functional groups can affect the compound's polarity, stability, and interaction with biological targets. Additionally, the thiophene moiety is known for its electronic properties, making such compounds of interest in materials science and organic electronics. Overall, methyl 2-amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxylate exemplifies a complex organic structure with diverse potential applications.

methyl 2-amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxylate

350997-34-1: Methyl 2-amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxylate, with the CAS number 350997-34-1, is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group and a carboxylate ester, contributing to its potential reactivity and solubility properties. The presence of the methyl and phenyl substituents enhances its lipophilicity and may influence its biological activity. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The specific arrangement of functional groups can affect the compound's polarity, stability, and interaction with biological targets. Additionally, the thiophene moiety is known for its electronic properties, making such compounds of interest in materials science and organic electronics. Overall, methyl 2-amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxylate exemplifies a complex organic structure with diverse potential applications.

CAS 350997-34-1

methyl 2-amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxylate

2-Amino-5-methyl-4-p-tolylthiophene-3-carboxylic acid methyl ester

Ref: 10-F014069