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CAS 2044713-63-3

:

5-(Aminocarbonyl)-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinepropanoic acid

Description:
5-(Aminocarbonyl)-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinepropanoic acid is a pyrimidine derivative characterized by its unique structural features, including a pyrimidine ring with two carbonyl groups and an amino acid side chain. This compound typically exhibits properties such as solubility in polar solvents, which is common for compounds containing carboxylic acid and amine functional groups. The presence of the dioxo and aminocarbonyl groups suggests potential reactivity, particularly in forming hydrogen bonds and participating in various chemical reactions, including nucleophilic attacks and condensation reactions. Its molecular structure may confer biological activity, making it of interest in pharmaceutical research. The compound's stability can be influenced by pH and temperature, and it may undergo degradation under extreme conditions. Overall, this substance represents a class of compounds that could have applications in medicinal chemistry, particularly in the development of therapeutics targeting specific biological pathways.
Formula:C8H9N3O5
InChI:InChI=1S/C8H9N3O5/c9-6(14)4-3-11(2-1-5(12)13)8(16)10-7(4)15/h3H,1-2H2,(H2,9,14)(H,12,13)(H,10,15,16)
InChI key:InChIKey=OAXBOGYHWRIZEN-UHFFFAOYSA-N
SMILES:C(CC(O)=O)N1C=C(C(N)=O)C(=O)NC1=O
Synonyms:
  • 1(2H)-Pyrimidinepropanoic acid, 5-(aminocarbonyl)-3,4-dihydro-2,4-dioxo-
  • 5-(Aminocarbonyl)-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinepropanoic acid
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