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CAS 24242-18-0

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5-(Aminocarbonyl)-2-pyridinecarboxylic acid

Description:
5-(Aminocarbonyl)-2-pyridinecarboxylic acid, also known as a pyridine derivative, is characterized by its functional groups, which include an amino group and a carboxylic acid group attached to a pyridine ring. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar solvents due to the presence of the carboxylic acid and amino groups. It may participate in various chemical reactions, including amide formation and esterification, owing to its reactive functional groups. The presence of the pyridine ring contributes to its aromaticity, which can influence its stability and reactivity. This compound may also exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for hydrogen bonding, which can affect its interactions in biological systems. Overall, 5-(Aminocarbonyl)-2-pyridinecarboxylic acid is a versatile compound with potential applications in medicinal chemistry and organic synthesis.
Formula:C7H6N2O3
InChI:InChI=1S/C7H6N2O3/c8-6(10)4-1-2-5(7(11)12)9-3-4/h1-3H,(H2,8,10)(H,11,12)
InChI key:InChIKey=KGBSMDOELQXOBN-UHFFFAOYSA-N
SMILES:C(N)(=O)C=1C=CC(C(O)=O)=NC1
Synonyms:
  • 5-(Aminocarbonyl)-2-pyridinecarboxylic acid
  • 2-Pyridinecarboxylic acid, 5-(aminocarbonyl)-
  • Picolinic acid, 5-carbamoyl-
  • 5-Carboxamidopicolinic acid
  • 5-Carbamoylpicolinic acid
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