Ethyl 4-(2-chloropyridin-3-yl)-4-oxobutanoate, identified by its CAS number 852063-32-2, is an organic compound characterized by its ester functional group and a pyridine ring substituted with a chlorine atom. This compound features a butanoate backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the 2-chloropyridine moiety suggests that it may exhibit biological activity, making it of interest in medicinal chemistry. Ethyl 4-(2-chloropyridin-3-yl)-4-oxobutanoate is likely to be a solid or liquid at room temperature, depending on its molecular structure and intermolecular interactions. Its solubility in organic solvents, such as ethanol or dichloromethane, is expected, while its solubility in water may be limited due to the hydrophobic nature of the butanoate group. The compound's reactivity can be influenced by the electron-withdrawing effects of the chlorine atom, which may affect its behavior in chemical reactions, including nucleophilic substitutions and condensation reactions.

ethyl 4-(2-chloropyridin-3-yl)-4-oxobutanoate

852063-32-2: Ethyl 4-(2-chloropyridin-3-yl)-4-oxobutanoate, identified by its CAS number 852063-32-2, is an organic compound characterized by its ester functional group and a pyridine ring substituted with a chlorine atom. This compound features a butanoate backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the 2-chloropyridine moiety suggests that it may exhibit biological activity, making it of interest in medicinal chemistry. Ethyl 4-(2-chloropyridin-3-yl)-4-oxobutanoate is likely to be a solid or liquid at room temperature, depending on its molecular structure and intermolecular interactions. Its solubility in organic solvents, such as ethanol or dichloromethane, is expected, while its solubility in water may be limited due to the hydrophobic nature of the butanoate group. The compound's reactivity can be influenced by the electron-withdrawing effects of the chlorine atom, which may affect its behavior in chemical reactions, including nucleophilic substitutions and condensation reactions.

CAS 852063-32-2

ethyl 4-(2-chloropyridin-3-yl)-4-oxobutanoate

Ethyl 4-(2-chloro-3-pyridyl)-4-oxobutyrate

Ref: 10-F202272