2-Chloro-3-(chloromethyl)-5,7-dimethyl-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. This compound features two methyl groups at the 5 and 7 positions, contributing to its hydrophobic character and potentially influencing its biological activity. The presence of chlorine substituents at the 2 and 3 positions enhances its reactivity and may impart specific pharmacological properties. The chloromethyl group at the 3 position can serve as a reactive site for further chemical modifications or interactions with biological targets. This compound may exhibit interesting properties in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with various biological systems. Its CAS number, 948290-59-3, allows for easy identification and retrieval of information regarding its synthesis, applications, and safety data. As with many chlorinated compounds, considerations regarding environmental impact and toxicity are essential in its handling and application.

2-chloro-3-(chloromethyl)-5,7-dimethyl-quinoline

948290-59-3: 2-Chloro-3-(chloromethyl)-5,7-dimethyl-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. This compound features two methyl groups at the 5 and 7 positions, contributing to its hydrophobic character and potentially influencing its biological activity. The presence of chlorine substituents at the 2 and 3 positions enhances its reactivity and may impart specific pharmacological properties. The chloromethyl group at the 3 position can serve as a reactive site for further chemical modifications or interactions with biological targets. This compound may exhibit interesting properties in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with various biological systems. Its CAS number, 948290-59-3, allows for easy identification and retrieval of information regarding its synthesis, applications, and safety data. As with many chlorinated compounds, considerations regarding environmental impact and toxicity are essential in its handling and application.

<p>2-Chloro-3-chloromethyl-5,7-dimethylquinoline</p>

CAS 948290-59-3

2-chloro-3-(chloromethyl)-5,7-dimethyl-quinoline

2-Chloro-3-chloromethyl-5,7-dimethylquinoline

Ref: 54-OR307904