Methyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate, with the CAS number 350989-87-6, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylate functional group, which contributes to its potential as a building block in organic synthesis and medicinal chemistry. The presence of an amino group indicates that it may exhibit basic properties and could participate in various chemical reactions, such as nucleophilic substitutions. The methoxyphenyl substituent enhances its lipophilicity and may influence its biological activity. Additionally, the methyl groups attached to the thiophene ring can affect the compound's steric properties and overall reactivity. This compound may be of interest in the development of pharmaceuticals or agrochemicals due to its unique structural features, which could impart specific biological activities or enhance solubility in organic solvents. Overall, its diverse functional groups and aromatic characteristics make it a versatile compound in chemical research.

methyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate

350989-87-6: Methyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate, with the CAS number 350989-87-6, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylate functional group, which contributes to its potential as a building block in organic synthesis and medicinal chemistry. The presence of an amino group indicates that it may exhibit basic properties and could participate in various chemical reactions, such as nucleophilic substitutions. The methoxyphenyl substituent enhances its lipophilicity and may influence its biological activity. Additionally, the methyl groups attached to the thiophene ring can affect the compound's steric properties and overall reactivity. This compound may be of interest in the development of pharmaceuticals or agrochemicals due to its unique structural features, which could impart specific biological activities or enhance solubility in organic solvents. Overall, its diverse functional groups and aromatic characteristics make it a versatile compound in chemical research.

CAS 350989-87-6

methyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate

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

Ref: 10-F014072