Methyl 2-amino-4-(2,4-dimethylphenyl)-5-methylthiophene-3-carboxylate, with the CAS number 351156-17-7, is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and a carboxylate ester. This compound features a methyl group and a dimethylphenyl substituent, contributing to its hydrophobic characteristics. The presence of the amino group suggests potential for hydrogen bonding, which may influence its solubility and reactivity. The thiophene ring is known for its aromatic properties, which can impart stability and influence electronic interactions. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its properties can be further explored through spectroscopic methods. Overall, this compound represents a unique combination of functional groups that may lead to diverse applications in medicinal chemistry and materials science.

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

351156-17-7: Methyl 2-amino-4-(2,4-dimethylphenyl)-5-methylthiophene-3-carboxylate, with the CAS number 351156-17-7, is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and a carboxylate ester. This compound features a methyl group and a dimethylphenyl substituent, contributing to its hydrophobic characteristics. The presence of the amino group suggests potential for hydrogen bonding, which may influence its solubility and reactivity. The thiophene ring is known for its aromatic properties, which can impart stability and influence electronic interactions. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its properties can be further explored through spectroscopic methods. Overall, this compound represents a unique combination of functional groups that may lead to diverse applications in medicinal chemistry and materials science.

CAS 351156-17-7

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

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

Ref: 10-F014082