Ethyl 2-amino-4-(3,4-dimethylphenyl)-5-methylthiophene-3-carboxylate is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and an ester functional group. The presence of the ethyl ester indicates that it is likely to be a liquid at room temperature, with potential solubility in organic solvents. The thiophene ring contributes to its aromatic properties, while the dimethylphenyl substituent enhances its hydrophobic characteristics. This compound may exhibit biological activity due to the amino group, which can participate in various chemical reactions, including hydrogen bonding and nucleophilic attacks. Its unique structure suggests potential applications in pharmaceuticals or as a building block in organic synthesis. The compound's CAS number, 438220-53-2, allows for easy identification in chemical databases, facilitating research and development in various fields, including medicinal chemistry and materials science. Overall, this compound's distinctive features make it a subject of interest for further study and application.

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

438220-53-2: Ethyl 2-amino-4-(3,4-dimethylphenyl)-5-methylthiophene-3-carboxylate is a chemical compound characterized by its complex structure, which includes a thiophene ring, an amino group, and an ester functional group. The presence of the ethyl ester indicates that it is likely to be a liquid at room temperature, with potential solubility in organic solvents. The thiophene ring contributes to its aromatic properties, while the dimethylphenyl substituent enhances its hydrophobic characteristics. This compound may exhibit biological activity due to the amino group, which can participate in various chemical reactions, including hydrogen bonding and nucleophilic attacks. Its unique structure suggests potential applications in pharmaceuticals or as a building block in organic synthesis. The compound's CAS number, 438220-53-2, allows for easy identification in chemical databases, facilitating research and development in various fields, including medicinal chemistry and materials science. Overall, this compound's distinctive features make it a subject of interest for further study and application.

CAS 438220-53-2

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

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

Ref: IN-DA00DD1O

2-Amino-4-(3,4-dimethyl-phenyl)-5-methyl-thiophene-3-carboxylic acid ethyl ester

Ref: 10-F030576