4-Ethyl 2-(2-methoxyethyl) 5-amino-3-methylthiophene-2,4-dicarboxylate, identified by its CAS number 556016-30-9, is a synthetic organic compound characterized by its complex thiophene structure, which includes multiple functional groups. The presence of an ethyl group and a methoxyethyl substituent contributes to its hydrophobic and hydrophilic properties, respectively, potentially influencing its solubility in various solvents. The amino group is likely to impart basic characteristics, while the dicarboxylate moiety suggests the compound can participate in acid-base reactions and may form salts. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific pathways. Its structural features suggest potential applications in organic synthesis and materials science, where thiophene derivatives are often utilized for their electronic properties. Overall, the compound's unique combination of functional groups and structural characteristics positions it as a versatile candidate for further study in various chemical and biological contexts.

4-ETHYL 2-(2-METHOXYETHYL) 5-AMINO-3-METHYLTHIOPHENE-2,4-DICARBOXYLATE

556016-30-9: 4-Ethyl 2-(2-methoxyethyl) 5-amino-3-methylthiophene-2,4-dicarboxylate, identified by its CAS number 556016-30-9, is a synthetic organic compound characterized by its complex thiophene structure, which includes multiple functional groups. The presence of an ethyl group and a methoxyethyl substituent contributes to its hydrophobic and hydrophilic properties, respectively, potentially influencing its solubility in various solvents. The amino group is likely to impart basic characteristics, while the dicarboxylate moiety suggests the compound can participate in acid-base reactions and may form salts. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific pathways. Its structural features suggest potential applications in organic synthesis and materials science, where thiophene derivatives are often utilized for their electronic properties. Overall, the compound's unique combination of functional groups and structural characteristics positions it as a versatile candidate for further study in various chemical and biological contexts.

CAS 556016-30-9

4-ETHYL 2-(2-METHOXYETHYL) 5-AMINO-3-METHYLTHIOPHENE-2,4-DICARBOXYLATE

4-Ethyl 2-(2-methoxyethyl) 5-amino-3-methylthiophene-2,4-dicarboxylate

Ref: 3D-GXA01630