Methyl 3-amino-5-(4-bromophenyl)thiophene-2-carboxylate is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylate group, which contributes to its acidic properties, and an amino group that can participate in hydrogen bonding and nucleophilic reactions. The presence of the 4-bromophenyl substituent enhances its electronic properties and may influence its reactivity and solubility. Typically, compounds like this are of interest in medicinal chemistry and materials science due to their potential biological activity and utility in synthesizing more complex molecules. The molecular structure suggests that it may exhibit properties such as moderate to high lipophilicity, which can affect its bioavailability and interaction with biological targets. Additionally, the bromine atom can serve as a site for further chemical modification, making it a versatile building block in organic synthesis. Overall, this compound exemplifies the diverse functionalities that can be achieved through careful molecular design.

methyl 3-amino-5-(4-bromophenyl)thiophene-2-carboxylate

91076-95-8: Methyl 3-amino-5-(4-bromophenyl)thiophene-2-carboxylate is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylate group, which contributes to its acidic properties, and an amino group that can participate in hydrogen bonding and nucleophilic reactions. The presence of the 4-bromophenyl substituent enhances its electronic properties and may influence its reactivity and solubility. Typically, compounds like this are of interest in medicinal chemistry and materials science due to their potential biological activity and utility in synthesizing more complex molecules. The molecular structure suggests that it may exhibit properties such as moderate to high lipophilicity, which can affect its bioavailability and interaction with biological targets. Additionally, the bromine atom can serve as a site for further chemical modification, making it a versatile building block in organic synthesis. Overall, this compound exemplifies the diverse functionalities that can be achieved through careful molecular design.

CAS 91076-95-8

methyl 3-amino-5-(4-bromophenyl)thiophene-2-carboxylate

3-Amino-5-(4-bromophenyl)thiophene-2-carboxylic acid methyl ester

Ref: 10-F019540

Methyl 2-amino-4-(4-bromophenyl)thiophene-3-carboxylate

Ref: 3D-RDA07695