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CAS 22280-60-0

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6-Chloro-2-methyl-3-nitropyridine

Description:
6-Chloro-2-methyl-3-nitropyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom, a methyl group, and a nitro group. The presence of these functional groups imparts distinct chemical properties to the compound. The chlorine atom, being electronegative, can influence the reactivity and polarity of the molecule, while the nitro group is known for its strong electron-withdrawing effects, which can enhance the compound's acidity and reactivity in electrophilic substitution reactions. The methyl group contributes to the overall hydrophobic character of the molecule. This compound is typically used in various chemical syntheses and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its structure allows for potential applications in medicinal chemistry, particularly in the development of compounds with biological activity. As with many nitro-substituted compounds, it is important to handle 6-Chloro-2-methyl-3-nitropyridine with care due to potential toxicity and environmental concerns associated with nitro groups.
Formula:C6H5ClN2O2
InChI:InChI=1S/C6H5ClN2O2/c1-4-5(9(10)11)2-3-6(7)8-4/h2-3H,1H3
InChI key:InChIKey=GHSRMSJVYMITDX-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(C)N=C(Cl)C=C1
Synonyms:
  • 2-Chloro-5-Nitro-6-Methylpyridine
  • 2-Chloro-5-nitro-6-picoline
  • 2-Picoline, 6-chloro-3-nitro-
  • 3-Nitro-6-chloro-2-picoline
  • 6-Chloro-2-methyl-3-nitro-pyridine
  • 6-Chloro-2-methyl-3-nitropyridine
  • 6-Chloro-3-nitro-2-picoline
  • NSC 75592
  • Pyridine, 6-chloro-2-methyl-3-nitro-
  • 2-Chloro-6-methyl-5-nitropyridine
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