2-Chloro-6,8-dimethylquinoline-3-carbonitrile is a chemical compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. The presence of the chloro group at the 2-position and two methyl groups at the 6 and 8 positions contributes to its unique reactivity and physical properties. The carbonitrile functional group at the 3-position enhances its potential for nucleophilic reactions and increases its polarity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The presence of halogen and cyano groups can also influence its biological activity, making it of interest in medicinal chemistry. As with many quinoline derivatives, it may exhibit various biological properties, including antimicrobial or antitumor activities, although specific biological data would need to be referenced for detailed insights. Safety and handling precautions should be observed due to the potential toxicity associated with halogenated compounds.

2-chloro-6,8-dimethylquinoline-3-carbonitrile

917750-50-6: 2-Chloro-6,8-dimethylquinoline-3-carbonitrile is a chemical compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. The presence of the chloro group at the 2-position and two methyl groups at the 6 and 8 positions contributes to its unique reactivity and physical properties. The carbonitrile functional group at the 3-position enhances its potential for nucleophilic reactions and increases its polarity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The presence of halogen and cyano groups can also influence its biological activity, making it of interest in medicinal chemistry. As with many quinoline derivatives, it may exhibit various biological properties, including antimicrobial or antitumor activities, although specific biological data would need to be referenced for detailed insights. Safety and handling precautions should be observed due to the potential toxicity associated with halogenated compounds.

2-Chloro-6,8-dimethylquinoline-3-carbonitrile

CAS 917750-50-6

2-chloro-6,8-dimethylquinoline-3-carbonitrile

2-Chloro-6,8-dimethylquinoline-3-carbonitrile

Ref: 54-OR309452