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CAS 27582-14-5

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2-Methyl-3-nitro-4-pyridinamine

Description:
2-Methyl-3-nitro-4-pyridinamine, with the CAS number 27582-14-5, is an organic compound that features a pyridine ring substituted with both a methyl group and a nitro group, along with an amino group. This compound typically appears as a solid and is characterized by its aromatic nature due to the presence of the pyridine ring, which 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 reactivity and stability. Additionally, the amino group can participate in hydrogen bonding, enhancing solubility in polar solvents. The presence of these functional groups suggests that 2-Methyl-3-nitro-4-pyridinamine may exhibit biological activity, making it of interest for further research in medicinal chemistry. Safety data should be consulted for handling and storage, as nitro compounds can be sensitive to heat and shock.
Formula:C6H7N3O2
InChI:InChI=1S/C6H7N3O2/c1-4-6(9(10)11)5(7)2-3-8-4/h2-3H,1H3,(H2,7,8)
InChI key:InChIKey=PWMOQGXCXFHJMF-UHFFFAOYSA-N
SMILES:N(=O)(=O)C=1C(N)=CC=NC1C
Synonyms:
  • 2-Methyl-3-nitro-4-pyridinamine
  • 2-Methyl-3-nitropyridin-4-amine
  • 2-Picoline, 4-amino-3-nitro-
  • 2-Picoline,4-amino-3-nitro- (8CI)
  • 4-Amino-2-methyl-3-nitropyridine
  • 4-Pyridinamine, 2-methyl-3-nitro-
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