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CAS 76470-35-4

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1,6-Dihydro-5-hydroxy-6-oxo-3-pyridinecarboxylic acid

Description:
1,6-Dihydro-5-hydroxy-6-oxo-3-pyridinecarboxylic acid, also known as a derivative of pyridinecarboxylic acid, is characterized by its unique structural features that include a pyridine ring and multiple functional groups. This compound typically exhibits a carboxylic acid group, a hydroxyl group, and a keto group, contributing to its acidic and potentially chelating properties. It is often studied for its biological activity, including potential roles in metabolic pathways or as a precursor in synthetic chemistry. The presence of the hydroxyl and keto groups can enhance its reactivity, making it useful in various chemical reactions, including esterification and condensation. Additionally, its solubility in polar solvents suggests it may interact favorably with biological systems. The compound's CAS number, 76470-35-4, allows for precise identification in chemical databases, facilitating research and application in fields such as pharmaceuticals, agrochemicals, and materials science. Overall, this compound's diverse functional groups and structural characteristics make it a subject of interest in both academic and industrial chemistry.
Formula:C6H5NO4
InChI:InChI=1S/C6H5NO4/c8-4-1-3(6(10)11)2-7-5(4)9/h1-2,8H,(H,7,9)(H,10,11)
InChI key:InChIKey=GNZULNKSXZNZBO-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=C(O)C(=O)NC1
Synonyms:
  • 1,6-Dihydro-5-hydroxy-6-oxo-3-pyridinecarboxylic acid
  • 3-Pyridinecarboxylic Acid, 1,6-Dihydro-5-Hydroxy-6-Oxo-
  • 5-Hydroxy-6-oxo-1,6-dihydropyridine-3-carboxylic acid
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