2,6-Dimethoxy-3-nitropyridine is an organic compound characterized by its pyridine ring substituted with two methoxy groups and one nitro group. The presence of the methoxy groups at the 2 and 6 positions enhances the compound's solubility in organic solvents and can influence its reactivity and interaction with other chemical species. The nitro group at the 3 position introduces significant electron-withdrawing characteristics, which can affect the compound's acidity and reactivity in electrophilic aromatic substitution reactions. This compound typically appears as a yellow to orange solid and is used in various chemical syntheses, including the preparation of pharmaceuticals and agrochemicals. Its molecular structure contributes to its potential applications in medicinal chemistry, particularly in the development of compounds with biological activity. Additionally, safety data should be considered, as nitro compounds can be sensitive and may require careful handling due to potential toxicity or environmental impact.

2,6-dimethoxy-3-nitropyridine

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2,6-Dimethoxy-3-nitropyridine is a heteroaromatic compound that can be synthesized by reacting benzene with nitric acid. It is a conjugate acid of pyridine. 2,6-Dimethoxy-3-nitropyridine has been shown to react with electrophiles via nitration and also undergoes homolytic cleavage. This compound reacts with nitronium ion to form a heteroaromatic compound.

CAS 18677-41-3: 2,6-dimethoxy-3-nitropyridine

2,6-Dimethoxy-3-nitropyridine

Ref: 3D-FD152759

2,6-Dimethoxy-3-nitropyridine

Ref: 10-F222608

2,6-DIMETHOXY-3-NITROPYRIDINE

Ref: IN-DA00APH9

2,6-Dimethoxy-3-nitropyridine

Ref: 54-OR5849