Methyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate, with the CAS number 350990-17-9, 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 and a carboxylate ester, contributing to its potential reactivity and solubility in various solvents. The presence of the 2,5-dimethylphenyl substituent enhances its hydrophobic characteristics and may influence its biological activity. The methyl groups attached to the thiophene and the phenyl ring can affect the compound's steric properties and electronic distribution, potentially impacting its interactions in chemical reactions or biological systems. Methyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate may be of interest in medicinal chemistry and material science due to its unique structural features, which could lead to applications in drug development or as a building block in organic synthesis. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

methyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate

350990-17-9: Methyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate, with the CAS number 350990-17-9, 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 and a carboxylate ester, contributing to its potential reactivity and solubility in various solvents. The presence of the 2,5-dimethylphenyl substituent enhances its hydrophobic characteristics and may influence its biological activity. The methyl groups attached to the thiophene and the phenyl ring can affect the compound's steric properties and electronic distribution, potentially impacting its interactions in chemical reactions or biological systems. Methyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate may be of interest in medicinal chemistry and material science due to its unique structural features, which could lead to applications in drug development or as a building block in organic synthesis. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

CAS 350990-17-9

methyl 2-amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylate

2-Amino-4-(2,5-dimethylphenyl)-5-methylthiophene-3-carboxylic acid methyl ester

Ref: 10-F014083