3-Methyl-5-nitro-4-pyridinamine, with the CAS number 18227-67-3, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a methyl group and a nitro group attached to the pyridine ring, specifically at the 3 and 5 positions, respectively, while an amino group is present at the 4 position. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The nitro group is known for its electron-withdrawing properties, which can influence the compound's acidity and reactivity. Additionally, the amino group can participate in hydrogen bonding, affecting the compound's solubility and interaction with biological systems. Overall, 3-Methyl-5-nitro-4-pyridinamine is a compound of interest due to its unique structural features and potential utility in synthetic chemistry and medicinal applications.

3-Methyl-5-nitro-4-pyridinamine

18227-67-3: 3-Methyl-5-nitro-1,4-dihydropyridin-4-imine, 3-Methyl-5-nitro-4-pyridinamine, 3-Methyl-5-nitropyridin-4-amine, 3-Picoline, 4-amino-5-nitro-,  4-pyridinamine, 3-methyl-5-nitro-, 4-Pyridinamine, 3-methyl-5-nitro-

CAS 18227-67-3: 3-Methyl-5-nitro-4-pyridinamine

4-Amino-5-methyl-3-nitropyridine

Ref: 10-F223385

4-Amino-5-methyl-3-nitropyridine

Ref: 3D-TAA22767

4-Pyridinamine, 3-methyl-5-nitro-

Ref: IN-DA0023K7

4-Amino-5-methyl-3-nitropyridine

Ref: 54-OR345284