Ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate is a chemical compound characterized by its complex structure, which includes an ethyl ester functional group and an aromatic amine moiety. The presence of halogen substituents, specifically chlorine and iodine, on the aromatic ring contributes to its unique reactivity and potential biological activity. The methoxy group enhances the compound's lipophilicity, which may influence its solubility and permeability in biological systems. This compound is likely to exhibit specific interactions with biological targets, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with antimicrobial or anticancer properties. Additionally, the presence of both electron-withdrawing and electron-donating groups can affect its electronic properties, influencing its behavior in chemical reactions. Overall, ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate represents a versatile scaffold for further chemical modifications and investigations in various fields of research.

ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate

1508278-50-9: Ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate is a chemical compound characterized by its complex structure, which includes an ethyl ester functional group and an aromatic amine moiety. The presence of halogen substituents, specifically chlorine and iodine, on the aromatic ring contributes to its unique reactivity and potential biological activity. The methoxy group enhances the compound's lipophilicity, which may influence its solubility and permeability in biological systems. This compound is likely to exhibit specific interactions with biological targets, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with antimicrobial or anticancer properties. Additionally, the presence of both electron-withdrawing and electron-donating groups can affect its electronic properties, influencing its behavior in chemical reactions. Overall, ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate represents a versatile scaffold for further chemical modifications and investigations in various fields of research.

CAS 1508278-50-9

ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate

Ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate

Ref: IN-DA00ABRO