2-Chloro-4,6-dimethyl-5-nitropyridine-3-carbonitrile is a heterocyclic organic compound characterized by its pyridine ring, which is substituted at various positions. The presence of a chlorine atom at the 2-position, two methyl groups at the 4 and 6 positions, a nitro group at the 5-position, and a cyano group at the 3-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential reactivity due to the electron-withdrawing nature of the nitro and cyano groups, which can influence its behavior in chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions. Additionally, the presence of multiple functional groups may impart biological activity, making it of interest in pharmaceutical research. Safety data should be consulted, as compounds with nitro and halogen substituents can pose health risks and environmental concerns. Overall, 2-chloro-4,6-dimethyl-5-nitropyridine-3-carbonitrile is a complex molecule with diverse applications in organic synthesis and medicinal chemistry.

2-chloro-4,6-dimethyl-5-nitropyridine-3-carbonitrile

6220-77-5: 2-Chloro-4,6-dimethyl-5-nitropyridine-3-carbonitrile is a heterocyclic organic compound characterized by its pyridine ring, which is substituted at various positions. The presence of a chlorine atom at the 2-position, two methyl groups at the 4 and 6 positions, a nitro group at the 5-position, and a cyano group at the 3-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential reactivity due to the electron-withdrawing nature of the nitro and cyano groups, which can influence its behavior in chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions. Additionally, the presence of multiple functional groups may impart biological activity, making it of interest in pharmaceutical research. Safety data should be consulted, as compounds with nitro and halogen substituents can pose health risks and environmental concerns. Overall, 2-chloro-4,6-dimethyl-5-nitropyridine-3-carbonitrile is a complex molecule with diverse applications in organic synthesis and medicinal chemistry.

2-Chloro-3-cyano-4,6-dimethyl-5-nitropyridine

CAS 6220-77-5

2-chloro-4,6-dimethyl-5-nitropyridine-3-carbonitrile

2-Chloro-3-cyano-4,6-dimethyl-5-nitropyridine

Ref: 54-OR300753