4,8-Dimethylquinolin-2(1H)-one, with the CAS number 5349-78-0, is a heterocyclic organic compound belonging to the quinoline family. This compound features a quinoline backbone, which consists of a fused benzene and pyridine ring, and is substituted at the 4 and 8 positions with methyl groups, as well as a carbonyl group at the 2 position, contributing to its classification as a quinolinone. It typically appears as a solid at room temperature and is characterized by its aromatic nature, which imparts stability and unique chemical reactivity. The presence of the carbonyl group allows for potential interactions in various chemical reactions, including nucleophilic attacks and condensation reactions. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its solubility can vary depending on the solvent, and it may be used in various applications, including as a building block in organic synthesis or as a potential pharmaceutical agent. Safety data should be consulted for handling and usage guidelines.

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

5349-78-0: 2(1H)-quinolinone, 4,8-dimethyl-, 2-Quinolinol, 4,8-Dimethyl-, 4,8-Dimethylquinolin-2-Ol

4,8-DIMETHYL-2-QUINOLINOL

4,8-Dimethylquinolin-2(1H)-one is a quinone that has been synthesized by the reaction of 2-phenylbenzothiazole with diborane. This molecule has shown anti-cancer activity in vitro. 4,8-Dimethylquinolin-2(1H)-one is a heterocycle that can be synthesized from 2-phenylbenzothiazole and diborane. The single-stranded DNA binding property of 4,8-dimethylquinolin-2(1H)-one is due to the presence of hydroxyl groups on the benzene ring. 4,8-Dimethylquinolin-2(1H)-one also has a high affinity for DNA and inhibits bacterial growth by binding to single stranded DNA (ssDNA).

CAS 5349-78-0: 4,8-dimethylquinolin-2(1H)-one

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

Ref: 10-F374097

4,8-DIMETHYL-2-QUINOLINOL

Ref: IN-DA00DIZ9

4,8-Dimethylquinolin-2(1H)-one

Ref: 3D-FD131937