6,8-Dichloro-2-methylquinolin-4(1H)-one is a synthetic organic compound belonging to the quinoline family, characterized by its fused bicyclic structure. This compound features two chlorine atoms at the 6 and 8 positions and a methyl group at the 2 position of the quinoline ring, along with a ketone functional group at the 4 position. It is typically a solid at room temperature and may exhibit a range of physical properties such as solubility in organic solvents, depending on its molecular interactions. The presence of chlorine substituents can influence its reactivity and biological activity, making it of interest in medicinal chemistry and material science. This compound may also exhibit fluorescence properties, which can be useful in various applications, including as a dye or in biological imaging. Its specific applications and behavior in chemical reactions would depend on the context of use, including potential roles in drug development or as a precursor in organic synthesis. Safety and handling precautions should be observed due to the presence of halogenated compounds, which can pose environmental and health risks.

6,8-dichloro-2-methylquinolin-4(1H)-one

95541-31-4: 6,8-Dichloro-2-methylquinolin-4(1H)-one is a synthetic organic compound belonging to the quinoline family, characterized by its fused bicyclic structure. This compound features two chlorine atoms at the 6 and 8 positions and a methyl group at the 2 position of the quinoline ring, along with a ketone functional group at the 4 position. It is typically a solid at room temperature and may exhibit a range of physical properties such as solubility in organic solvents, depending on its molecular interactions. The presence of chlorine substituents can influence its reactivity and biological activity, making it of interest in medicinal chemistry and material science. This compound may also exhibit fluorescence properties, which can be useful in various applications, including as a dye or in biological imaging. Its specific applications and behavior in chemical reactions would depend on the context of use, including potential roles in drug development or as a precursor in organic synthesis. Safety and handling precautions should be observed due to the presence of halogenated compounds, which can pose environmental and health risks.

CAS 95541-31-4

6,8-dichloro-2-methylquinolin-4(1H)-one

6,8-Dichloro-2-methylquinolin-4-ol

Ref: IN-DA01DWYT

6,8-Dichloro-4-hydroxy-2-methylquinoline

Ref: 54-OR307999