Ethyl 3-amino-6-chloropyridine-2-carboxylate is a chemical compound characterized by its pyridine ring structure, which includes an amino group and a chloro substituent. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the amino group suggests potential for hydrogen bonding and reactivity in various chemical reactions, such as nucleophilic substitutions. The chloro group can also influence the compound's reactivity, making it a useful intermediate in organic synthesis. Ethyl 3-amino-6-chloropyridine-2-carboxylate may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for potential interactions with biological targets, which could lead to applications in drug development. Additionally, the compound's properties, such as melting point, boiling point, and solubility, would depend on its specific molecular interactions and the presence of functional groups. Overall, this compound represents a versatile building block in organic chemistry and medicinal chemistry.

ethyl 3-amino-6-chloropyridine-2-carboxylate

1352200-86-2: Ethyl 3-amino-6-chloropyridine-2-carboxylate is a chemical compound characterized by its pyridine ring structure, which includes an amino group and a chloro substituent. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the amino group suggests potential for hydrogen bonding and reactivity in various chemical reactions, such as nucleophilic substitutions. The chloro group can also influence the compound's reactivity, making it a useful intermediate in organic synthesis. Ethyl 3-amino-6-chloropyridine-2-carboxylate may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for potential interactions with biological targets, which could lead to applications in drug development. Additionally, the compound's properties, such as melting point, boiling point, and solubility, would depend on its specific molecular interactions and the presence of functional groups. Overall, this compound represents a versatile building block in organic chemistry and medicinal chemistry.

CAS 1352200-86-2

ethyl 3-amino-6-chloropyridine-2-carboxylate

ethyl 3-amino-6-chloropyridine-2-carboxylate

Ref: IN-DA009XGI

Ethyl 3-amino-6-chloropicolinate

Ref: 54-OR1045776

Ethyl 3-amino-6-chloropicolinate

Ref: 10-F459014

Ethyl 3-Amino-6-chloropyridine-2-carboxylate

Ref: 3D-CEC20086