2-Methyl 4-propyl 5-amino-3-methylthiophene-2,4-dicarboxylate is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. This compound features multiple functional groups, including amino and carboxylate groups, which contribute to its reactivity and potential applications in organic synthesis and pharmaceuticals. The presence of methyl and propyl substituents on the thiophene ring enhances its hydrophobic characteristics, potentially influencing its solubility and interaction with biological systems. The dicarboxylate moiety suggests that this compound may participate in various chemical reactions, such as esterification or amidation, making it versatile in synthetic chemistry. Additionally, the amino group may provide sites for further functionalization, allowing for the development of derivatives with tailored properties. Overall, this compound's unique structure and functional groups position it as a candidate for research in medicinal chemistry and materials science.

2-methyl 4-propyl 5-amino-3-methylthiophene-2,4-dicarboxylate

438532-72-0: 2-Methyl 4-propyl 5-amino-3-methylthiophene-2,4-dicarboxylate is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. This compound features multiple functional groups, including amino and carboxylate groups, which contribute to its reactivity and potential applications in organic synthesis and pharmaceuticals. The presence of methyl and propyl substituents on the thiophene ring enhances its hydrophobic characteristics, potentially influencing its solubility and interaction with biological systems. The dicarboxylate moiety suggests that this compound may participate in various chemical reactions, such as esterification or amidation, making it versatile in synthetic chemistry. Additionally, the amino group may provide sites for further functionalization, allowing for the development of derivatives with tailored properties. Overall, this compound's unique structure and functional groups position it as a candidate for research in medicinal chemistry and materials science.

CAS 438532-72-0

2-methyl 4-propyl 5-amino-3-methylthiophene-2,4-dicarboxylate

5-Amino-3-methyl-thiophene-2,4-dicarboxylic acid 2-methyl ester 4-propyl ester

Ref: 10-F030597