8-Chloro-2-(chloromethyl)-1H-quinolin-4-one is a synthetic organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This compound features a chloro substituent at the 8-position and a chloromethyl group at the 2-position of the quinoline ring, contributing to its reactivity and potential biological activity. The presence of chlorine atoms enhances its lipophilicity and may influence its interaction with biological targets. Typically, quinoline derivatives exhibit a range of pharmacological properties, including antimicrobial, anti-inflammatory, and anticancer activities. The compound's molecular structure suggests it may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing nature of the chlorine substituents. Its CAS number, 946692-43-9, allows for precise identification in chemical databases and literature. Overall, 8-chloro-2-(chloromethyl)-1H-quinolin-4-one represents a compound of interest in medicinal chemistry and material science, warranting further investigation into its properties and potential applications.

8-chloro-2-(chloromethyl)-1H-quinolin-4-one

946692-43-9: 8-Chloro-2-(chloromethyl)-1H-quinolin-4-one is a synthetic organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This compound features a chloro substituent at the 8-position and a chloromethyl group at the 2-position of the quinoline ring, contributing to its reactivity and potential biological activity. The presence of chlorine atoms enhances its lipophilicity and may influence its interaction with biological targets. Typically, quinoline derivatives exhibit a range of pharmacological properties, including antimicrobial, anti-inflammatory, and anticancer activities. The compound's molecular structure suggests it may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing nature of the chlorine substituents. Its CAS number, 946692-43-9, allows for precise identification in chemical databases and literature. Overall, 8-chloro-2-(chloromethyl)-1H-quinolin-4-one represents a compound of interest in medicinal chemistry and material science, warranting further investigation into its properties and potential applications.

CAS 946692-43-9

8-chloro-2-(chloromethyl)-1H-quinolin-4-one

8-chloro-2-(chloromethyl)-4(1H)-quinolinone

Ref: 10-F310616