2,2,4-Trimethylquinolin-6(2H)-one, with the CAS number 4071-18-5, is an organic compound belonging to the quinoline family, characterized by a fused bicyclic structure that includes a benzene ring and a pyridine ring. This compound features three methyl groups at the 2, 2, and 4 positions of the quinoline structure, contributing to its unique properties. It is typically a yellow to brown solid at room temperature and is soluble in organic solvents. The presence of the carbonyl group at the 6-position enhances its reactivity, making it useful in various chemical reactions, including those involving nucleophiles. 2,2,4-Trimethylquinolin-6(2H)-one is of interest in the fields of organic synthesis and materials science, often serving as a precursor or intermediate in the synthesis of more complex molecules. Additionally, it may exhibit biological activity, which warrants further investigation for potential applications in pharmaceuticals or agrochemicals. Safety data should be consulted for handling and storage, as with all chemical substances.

2,2,4-trimethylquinolin-6(2H)-one

4071-18-5: 2,2,4-Trimethylquinolin-6(2H)-one, with the CAS number 4071-18-5, is an organic compound belonging to the quinoline family, characterized by a fused bicyclic structure that includes a benzene ring and a pyridine ring. This compound features three methyl groups at the 2, 2, and 4 positions of the quinoline structure, contributing to its unique properties. It is typically a yellow to brown solid at room temperature and is soluble in organic solvents. The presence of the carbonyl group at the 6-position enhances its reactivity, making it useful in various chemical reactions, including those involving nucleophiles. 2,2,4-Trimethylquinolin-6(2H)-one is of interest in the fields of organic synthesis and materials science, often serving as a precursor or intermediate in the synthesis of more complex molecules. Additionally, it may exhibit biological activity, which warrants further investigation for potential applications in pharmaceuticals or agrochemicals. Safety data should be consulted for handling and storage, as with all chemical substances.

Ethoxyquin quinone imine

Stability Light Sensitive Applications A metabolite of Ethoxyquin. An oxidation product of the antidegradant Ethoxyquin found in the muscle of Atlantic salmon. References Kahl, R., et al.: Toxicology, 28, 229 (1983), Burka, L., et al.: Xenobiotica, 26, 597 (1996), Bammler, T., et al.: Toxicol. Sci., 54, 30 (2000), Hayes, J., et al.: Cancer, 174, 103 (2001),

CAS 4071-18-5

2,2,4-trimethylquinolin-6(2H)-one

Ethoxyquin quinone imine

Ref: 04-C13310400

2,6-Dihydro-2,2,4-trimethyl-6-quinolone

Ref: TR-D449900