2-(Chloromethyl)-5,8-dimethyl-1H-quinolin-4-one is a chemical compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This substance features a chloromethyl group (-CH2Cl) at the 2-position and two methyl groups at the 5 and 8 positions of the quinoline ring. The presence of the chloromethyl group suggests potential reactivity, making it useful in various synthetic applications, including as an intermediate in organic synthesis. The compound's molecular structure contributes to its unique physical and chemical properties, such as solubility in organic solvents and potential biological activity. Quinoline derivatives are often studied for their pharmacological properties, including antimicrobial and antitumor activities. The specific characteristics, such as melting point, boiling point, and spectral data, would typically be determined through experimental methods and can vary based on purity and environmental conditions. Overall, this compound represents a class of heterocyclic compounds with significant relevance in medicinal chemistry and organic synthesis.

2-(chloromethyl)-5,8-dimethyl-1H-quinolin-4-one

946755-49-3: 2-(Chloromethyl)-5,8-dimethyl-1H-quinolin-4-one is a chemical compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This substance features a chloromethyl group (-CH2Cl) at the 2-position and two methyl groups at the 5 and 8 positions of the quinoline ring. The presence of the chloromethyl group suggests potential reactivity, making it useful in various synthetic applications, including as an intermediate in organic synthesis. The compound's molecular structure contributes to its unique physical and chemical properties, such as solubility in organic solvents and potential biological activity. Quinoline derivatives are often studied for their pharmacological properties, including antimicrobial and antitumor activities. The specific characteristics, such as melting point, boiling point, and spectral data, would typically be determined through experimental methods and can vary based on purity and environmental conditions. Overall, this compound represents a class of heterocyclic compounds with significant relevance in medicinal chemistry and organic synthesis.

CAS 946755-49-3

2-(chloromethyl)-5,8-dimethyl-1H-quinolin-4-one

2-(Chloromethyl)-5,8-dimethylquinolin-4(1H)-one

Ref: IN-DA005VVC

2-(chloromethyl)-5,8-dimethyl-4(1H)-quinolinone

Ref: 10-F310425