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CAS 4430-97-1

:

α-Amino-3,4-dioxo-1,5-cyclohexadiene-1-propanoic acid

Description:
α-Amino-3,4-dioxo-1,5-cyclohexadiene-1-propanoic acid, also known by its CAS number 4430-97-1, is an organic compound characterized by its unique bicyclic structure that includes both amino and dicarbonyl functional groups. This compound features a cyclohexadiene ring system, which contributes to its reactivity and potential applications in organic synthesis. The presence of the amino group indicates that it can participate in various biochemical processes, potentially acting as an intermediate in amino acid metabolism. The dioxo groups suggest that it may exhibit strong electrophilic properties, making it a candidate for nucleophilic attack in chemical reactions. Additionally, the propanoic acid moiety provides acidity, which can influence its solubility and reactivity in different environments. Overall, this compound's structural features suggest it may have applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis, although specific applications would depend on further research into its properties and reactivity.
Formula:C9H9NO4
InChI:InChI=1S/C9H9NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6H,3,10H2,(H,13,14)
InChI key:InChIKey=AHMIDUVKSGCHAU-UHFFFAOYSA-N
SMILES:C(C(C(O)=O)N)C1=CC(=O)C(=O)C=C1
Synonyms:
  • 1,5-Cyclohexadiene-1-alanine, 3,4-dioxo-
  • 1,5-Cyclohexadiene-1-propanoic acid, alpha-amino-3,4-dioxo-
  • 1,5-Cyclohexadiene-1-propanoic acid, α-amino-3,4-dioxo-
  • 2-Amino-3-(3,4-dioxo-1-cyclohexa-1,5-dienyl)-propanoic acid
  • 2-Amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoic acid
  • 3-(3,4-dioxocyclohexa-1,5-dien-1-yl)-L-alanine
  • α-Amino-3,4-dioxo-1,5-cyclohexadiene-1-propanoic acid
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