3-Bromo-4-chloro-8-methoxy-quinoline is a synthetic organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of bromine and chlorine substituents at the 3 and 4 positions, respectively, introduces significant reactivity and influences the compound's chemical properties, such as its polarity and solubility. The methoxy group at the 8 position enhances the compound's electron-donating characteristics, potentially affecting its biological activity and interaction with other molecules. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the presence of halogens can facilitate further chemical modifications, allowing for the synthesis of derivatives with varied properties. As with many quinoline derivatives, it may also exhibit fluorescence, which can be useful in analytical applications. Safety and handling precautions should be observed due to the presence of halogenated compounds, which can pose environmental and health risks.

3-bromo-4-chloro-8-methoxy-quinoline

142781-92-8: 3-Bromo-4-chloro-8-methoxy-quinoline is a synthetic organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of bromine and chlorine substituents at the 3 and 4 positions, respectively, introduces significant reactivity and influences the compound's chemical properties, such as its polarity and solubility. The methoxy group at the 8 position enhances the compound's electron-donating characteristics, potentially affecting its biological activity and interaction with other molecules. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the presence of halogens can facilitate further chemical modifications, allowing for the synthesis of derivatives with varied properties. As with many quinoline derivatives, it may also exhibit fluorescence, which can be useful in analytical applications. Safety and handling precautions should be observed due to the presence of halogenated compounds, which can pose environmental and health risks.

<p>3-Bromo-4-chloro-8-methoxyquinoline</p>

CAS 142781-92-8

3-bromo-4-chloro-8-methoxy-quinoline

3-Bromo-4-chloro-8-methoxyquinoline

Ref: 54-OR309334