Ethyl 2-amino-4-(3-bromophenyl)thiophene-3-carboxylate, with the CAS number 438218-48-5, is a chemical compound that features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound is characterized by the presence of an ethyl ester functional group, an amino group, and a bromophenyl substituent, which contribute to its potential biological activity and reactivity. The bromine atom in the para position of the phenyl ring enhances the compound's electrophilic character, making it useful in various synthetic applications. The thiophene moiety is known for its stability and ability to participate in various chemical reactions, including electrophilic substitution and coupling reactions. Ethyl 2-amino-4-(3-bromophenyl)thiophene-3-carboxylate may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its solubility and reactivity can vary based on the solvent and conditions used, which is important for its application in organic synthesis and potential drug development.

Ethyl 2-aMino-4-(3-broMophenyl)thiophene-3-carboxylate

438218-48-5: Ethyl 2-amino-4-(3-bromophenyl)thiophene-3-carboxylate, with the CAS number 438218-48-5, is a chemical compound that features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound is characterized by the presence of an ethyl ester functional group, an amino group, and a bromophenyl substituent, which contribute to its potential biological activity and reactivity. The bromine atom in the para position of the phenyl ring enhances the compound's electrophilic character, making it useful in various synthetic applications. The thiophene moiety is known for its stability and ability to participate in various chemical reactions, including electrophilic substitution and coupling reactions. Ethyl 2-amino-4-(3-bromophenyl)thiophene-3-carboxylate may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its solubility and reactivity can vary based on the solvent and conditions used, which is important for its application in organic synthesis and potential drug development.

CAS 438218-48-5

Ethyl 2-aMino-4-(3-broMophenyl)thiophene-3-carboxylate

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

Ref: IN-DA00D8KM