4,8-Dichloro-5-methoxy-2-methyl-quinoline is an organic compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. This compound features two chlorine substituents at the 4 and 8 positions, a methoxy group (-OCH3) at the 5 position, and a methyl group (-CH3) at the 2 position. These substituents contribute to its chemical reactivity and physical properties, such as solubility and boiling point. The presence of chlorine atoms typically enhances the compound's biological activity and can influence its interaction with various biological targets. The methoxy group can also affect the compound's electronic properties, potentially making it more lipophilic. 4,8-Dichloro-5-methoxy-2-methyl-quinoline may be of interest in medicinal chemistry and pharmacology due to its structural features, which could lead to applications in drug development or as a synthetic intermediate in organic synthesis. Its CAS number, 1206-61-7, allows for easy identification in chemical databases and literature.

4,8-dichloro-5-methoxy-2-methyl-quinoline

1206-61-7: 4,8-Dichloro-5-methoxy-2-methyl-quinoline is an organic compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. This compound features two chlorine substituents at the 4 and 8 positions, a methoxy group (-OCH3) at the 5 position, and a methyl group (-CH3) at the 2 position. These substituents contribute to its chemical reactivity and physical properties, such as solubility and boiling point. The presence of chlorine atoms typically enhances the compound's biological activity and can influence its interaction with various biological targets. The methoxy group can also affect the compound's electronic properties, potentially making it more lipophilic. 4,8-Dichloro-5-methoxy-2-methyl-quinoline may be of interest in medicinal chemistry and pharmacology due to its structural features, which could lead to applications in drug development or as a synthetic intermediate in organic synthesis. Its CAS number, 1206-61-7, allows for easy identification in chemical databases and literature.

CAS 1206-61-7

4,8-dichloro-5-methoxy-2-methyl-quinoline

4,8-Dichloro-5-methoxy-2-methylquinoline

Ref: 3D-BAA20661