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CAS 1053655-82-5

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2-Bromo-5-nitro-4-Pyridinecarboxylic acid

Description:
2-Bromo-5-nitro-4-pyridinecarboxylic acid is a heterocyclic organic compound characterized by the presence of a pyridine ring substituted with a bromine atom, a nitro group, and a carboxylic acid functional group. The bromine substitution typically enhances the compound's reactivity, making it useful in various synthetic applications. The nitro group, known for its electron-withdrawing properties, can influence the compound's acidity and reactivity, particularly in electrophilic aromatic substitution reactions. The carboxylic acid group contributes to the compound's acidic nature and solubility in polar solvents. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its structural features suggest potential applications in the development of agrochemicals or as intermediates in organic synthesis. Additionally, the presence of multiple functional groups allows for further derivatization, expanding its utility in chemical synthesis. As with many pyridine derivatives, it may also exhibit unique electronic properties, making it a subject of study in materials science and coordination chemistry.
Formula:C6H3BrN2O4
InChI:InChI=1S/C6H3BrN2O4/c7-5-1-3(6(10)11)4(2-8-5)9(12)13/h1-2H,(H,10,11)
InChI key:InChIKey=YISYYAZCRUHFBZ-UHFFFAOYSA-N
SMILES:N(=O)(=O)C=1C(C(O)=O)=CC(Br)=NC1
Synonyms:
  • 2-Bromo-5-nitro-4-Pyridinecarboxylic acid
  • 2-Bromo-5-nitro-4-Pyridinecarboxylic acid ISO 9001：2015 REACH
  • 2-broMo-5-nitropyridin-4-carboxylic acid
  • 2-bromo-5-nitropyridine-4-carboxylic acid
  • 4-Pyridinecarboxylic acid, 2-broMo-5-nitro-
  • 2-Bromo-5-nitro-4-pyridinecarboxylicaci
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