Ethyl 4-(2-chloropyridine-3-carbonyl)benzoate is an organic compound characterized by its ester functional group, which is derived from the reaction of benzoic acid and ethanol. The presence of a 2-chloropyridine moiety introduces both aromaticity and halogen substitution, which can influence the compound's reactivity and biological activity. This compound typically exhibits moderate to high lipophilicity due to its aromatic structure, making it soluble in organic solvents while having limited solubility in water. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as the chloropyridine group can serve as a pharmacophore or a site for further functionalization. Additionally, the compound may exhibit specific interactions with biological targets, influenced by the electronic effects of the chlorine atom and the spatial arrangement of the substituents. Overall, ethyl 4-(2-chloropyridine-3-carbonyl)benzoate is a versatile compound with potential utility in various chemical and biological applications.

ethyl 4-(2-chloropyridine-3-carbonyl)benzoate

760192-98-1: Ethyl 4-(2-chloropyridine-3-carbonyl)benzoate is an organic compound characterized by its ester functional group, which is derived from the reaction of benzoic acid and ethanol. The presence of a 2-chloropyridine moiety introduces both aromaticity and halogen substitution, which can influence the compound's reactivity and biological activity. This compound typically exhibits moderate to high lipophilicity due to its aromatic structure, making it soluble in organic solvents while having limited solubility in water. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as the chloropyridine group can serve as a pharmacophore or a site for further functionalization. Additionally, the compound may exhibit specific interactions with biological targets, influenced by the electronic effects of the chlorine atom and the spatial arrangement of the substituents. Overall, ethyl 4-(2-chloropyridine-3-carbonyl)benzoate is a versatile compound with potential utility in various chemical and biological applications.

CAS 760192-98-1

ethyl 4-(2-chloropyridine-3-carbonyl)benzoate

2-Chloro-3-(4-ethoxycarbonylbenzoyl)pyridine

Ref: 10-F202248