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1 References  














Carvonic acid






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From Wikipedia, the free encyclopedia
 


Carvonic acid
Names
IUPAC name

2-(4-Methyl-5-oxo-cyclohex-3-enyl)-acrylic acid

Identifiers

CAS Number

3D model (JSmol)

  • (S): Interactive image
  • ChemSpider
  • 27330305 (S) ☒N
  • PubChem CID

    CompTox Dashboard (EPA)

    • InChI=1S/C10H12O3/c1-6-3-4-8(5-9(6)11)7(2)10(12)13/h3,8H,2,4-5H2,1H3,(H,12,13)/t8-/m1/s1 ☒N

      Key: BPJKNHQCPHBIAR-MRVPVSSYSA-N ☒N

    • (S): InChI=1S/C10H12O3/c1-6-3-4-8(5-9(6)11)7(2)10(12)13/h3,8H,2,4-5H2,1H3,(H,12,13)/t8-/m0/s1

      Key: BPJKNHQCPHBIAR-QMMMGPOBSA-N

    • (R): CC1=CC[C@H](CC1=O)C(=C)C(=O)O

    • (S): CC1=CC[C@@H](CC1=O)C(=C)C(=O)O

    Properties

    Chemical formula

    C10H12O3
    Molar mass 180.20 g/mol

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Carvonic acid, or α-methylene-4-methyl-5-oxo-3-cyclohexene-1-acetic acid, is a terpenoid formed by metabolism of carvone in humans.[1]

    References

    [edit]
    1. ^ Engel, W. (2001). "In Vivo Studies on the Metabolism of the Monoterpenes S-(+)- and R-(−)-Carvone in Humans Using the Metabolism of Ingestion-Correlated Amounts (MICA) Approach". J. Agric. Food Chem. 49 (8): 4069–4075. doi:10.1021/jf010157q. PMID 11513712.


  • t
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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Carvonic_acid&oldid=903705703"

    Categories: 
    Carboxylic acids
    Monoterpenes
    Enones
    Cyclohexenes
    Ketone stubs
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