4-Chloro-6-methylquinoline-3-carbonitrile is a heterocyclic organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chloro group at the 4-position and a methyl group at the 6-position contributes to its unique chemical properties. The carbonitrile functional group at the 3-position enhances its reactivity, making it a valuable intermediate in organic synthesis. 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, and materials science due to its ability to participate in various chemical reactions, such as nucleophilic substitutions and cycloadditions. Additionally, the presence of halogen and cyano groups may impart specific biological activities, making it of interest in medicinal chemistry. As with many quinoline derivatives, it may also exhibit fluorescence properties, which can be useful in analytical applications. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity and environmental impact.

4-chloro-6-methylquinoline-3-carbonitrile

1016818-79-3: 4-Chloro-6-methylquinoline-3-carbonitrile is a heterocyclic organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chloro group at the 4-position and a methyl group at the 6-position contributes to its unique chemical properties. The carbonitrile functional group at the 3-position enhances its reactivity, making it a valuable intermediate in organic synthesis. 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, and materials science due to its ability to participate in various chemical reactions, such as nucleophilic substitutions and cycloadditions. Additionally, the presence of halogen and cyano groups may impart specific biological activities, making it of interest in medicinal chemistry. As with many quinoline derivatives, it may also exhibit fluorescence properties, which can be useful in analytical applications. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity and environmental impact.

CAS 1016818-79-3

4-chloro-6-methylquinoline-3-carbonitrile

4-Chloro-6-methylquinoline-3-carbonitrile

Ref: IN-DA00056N

4-Chloro-6-methylquinoline-3-carbonitrile

Ref: 3D-RQB81879