Ethyl 3-amino-4-chlorobenzo[b]thiophen-2-carboxylate is a chemical compound characterized by its unique structure, which includes a benzo[b]thiophene core, an ethyl ester functional group, and amino and chloro substituents. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as stability and potential reactivity due to the presence of the amino group, which can act as a nucleophile. The chloro substituent may influence the compound's reactivity and solubility in various solvents. Ethyl 3-amino-4-chlorobenzo[b]thiophen-2-carboxylate may also display biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in the synthesis of pharmaceuticals or agrochemicals. Additionally, the presence of the carboxylate group can enhance its solubility in polar solvents, while the thiophene ring may contribute to electronic properties that are beneficial in various chemical reactions. Overall, this compound exemplifies the complexity and versatility of organic molecules in chemical research and applications.

ethyl 3-amino-4-chlorobenzo[b]thiophen-2-carboxylate

67189-92-8: Ethyl 3-amino-4-chlorobenzo[b]thiophen-2-carboxylate is a chemical compound characterized by its unique structure, which includes a benzo[b]thiophene core, an ethyl ester functional group, and amino and chloro substituents. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as stability and potential reactivity due to the presence of the amino group, which can act as a nucleophile. The chloro substituent may influence the compound's reactivity and solubility in various solvents. Ethyl 3-amino-4-chlorobenzo[b]thiophen-2-carboxylate may also display biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in the synthesis of pharmaceuticals or agrochemicals. Additionally, the presence of the carboxylate group can enhance its solubility in polar solvents, while the thiophene ring may contribute to electronic properties that are beneficial in various chemical reactions. Overall, this compound exemplifies the complexity and versatility of organic molecules in chemical research and applications.

ETHYL 3-AMINO-4-CHLOROBENZO[B!THIOPHEN-2-CARBOXYLATE, 97

Ethyl 3-amino-4-chloro-1-benzothiophene-2-carboxylate

CAS 67189-92-8

ethyl 3-amino-4-chlorobenzo[b]thiophen-2-carboxylate

ETHYL 3-AMINO-4-CHLOROBENZO[B!THIOPHEN-2-CARBOXYLATE, 97

Ref: IN-DA00FODM

Ethyl 3-amino-4-chloro-1-benzothiophene-2-carboxylate

Ref: 54-OR110209

ethyl 3-amino-4-chloro-1-benzothiophene-2-carboxylate

Ref: 10-F518190