6-Methyl-4-nitropyridine-2-carbonitrile is a heterocyclic organic compound characterized by a pyridine ring substituted with a methyl group, a nitro group, and a cyano group. The presence of these functional groups imparts unique chemical properties to the compound. The methyl group enhances the lipophilicity of the molecule, while the nitro group contributes to its electron-withdrawing characteristics, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The cyano group introduces a strong electron-withdrawing effect, which can influence the reactivity and stability of the compound. This substance is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structural features suggest potential applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Additionally, the compound's reactivity can be explored in the development of new materials or as a building block in the synthesis of more complex molecules. Safety precautions should be observed when handling this compound due to the presence of the nitro group, which can pose health risks.

6-methyl-4-nitropyridine-2-carbonitrile

30235-12-2: 6-Methyl-4-nitropyridine-2-carbonitrile is a heterocyclic organic compound characterized by a pyridine ring substituted with a methyl group, a nitro group, and a cyano group. The presence of these functional groups imparts unique chemical properties to the compound. The methyl group enhances the lipophilicity of the molecule, while the nitro group contributes to its electron-withdrawing characteristics, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The cyano group introduces a strong electron-withdrawing effect, which can influence the reactivity and stability of the compound. This substance is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structural features suggest potential applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Additionally, the compound's reactivity can be explored in the development of new materials or as a building block in the synthesis of more complex molecules. Safety precautions should be observed when handling this compound due to the presence of the nitro group, which can pose health risks.

CAS 30235-12-2

6-methyl-4-nitropyridine-2-carbonitrile

6-Methyl-4-nitropicolinonitrile

Ref: IN-DA002ZCG

6-Methyl-4-nitropyridine-2-carbonitrile

Ref: 54-OR60089