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1 References  














Fenchone






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From Wikipedia, the free encyclopedia
 


Fenchone[1]
Names
IUPAC name

1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one

Other names

1,3,3-Trimethyl-2-norcamphanone

Identifiers

CAS Number

  • 4695-62-9D checkY
  • 7787-20-4L checkY
  • 3D model (JSmol)

    ChEBI
  • CHEBI:165D
  • CHEBI:36612L
  • ChemSpider
    ECHA InfoCard 100.013.458 Edit this at Wikidata
    KEGG

    PubChem CID

    UNII
  • S436YKU51N D checkY
  • K6G5Y2Y3Q2 L checkY
  • CompTox Dashboard (EPA)

    • InChI=1S/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3 checkY

      Key: LHXDLQBQYFFVNW-UHFFFAOYSA-N checkY

    • InChI=1/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3

      Key: LHXDLQBQYFFVNW-UHFFFAOYAX

    • O=C1C(C)(C)C2CC1(C)CC2

    Properties

    Chemical formula

    C10H16O
    Molar mass 152.23 g/mol
    Density 0.948 g/cm3
    Melting point 6.1 °C (43.0 °F; 279.2 K)
    Boiling point 193.5 °C (380.3 °F; 466.6 K)

    Refractive index (nD)

    1.4625

    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

    Fenchone is an organic compound classified as a monoterpenoid and a ketone. It is a colorless oily liquid. It has a structure and an odor similar to those of camphor. Fenchone is a constituent of absinthe and the essential oiloffennel. Fenchone is used as a flavor in foods and in perfumery.[2]

    Other names for fenchone include dl-fenchone and (±)-fenchone. It is a mixture of the enantiomers d-fenchone and l-fenchone. Other names for d-fenchone include (+)-fenchone and (1S,4R)-fenchone. Other names for l-fenchone include (−)-fenchone and (1R,4S)-fenchone. The d-fenchone enantiomer occurs in pure form in wild, bitter and sweet fennel plants and seeds, whereas the l-fenchone enantiomer occurs in pure form in wormwood, tansy, and cedarleaf.[3]

    References[edit]

    1. ^ Merck Index, 11th Edition, 3911.
  • ^ Karl-Georg Fahlbusch, Franz-Josef Hammerschmidt, Johannes Panten, Wilhelm Pickenhagen, Dietmar Schatkowski, Kurt Bauer, Dorothea Garbe, Horst Surburg "Flavors and Fragrances" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim: 2002. Published online: 15 January 2003; doi:10.1002/14356007.a11_141.
  • ^ U. Ravid, E. Putievsky, I. Katzir, R. Ikan “Chiral gc analysis of enantiomerically pure fenchone in essential oils” in Flavour and Fragrance Journal, 7: 169-172, John Wiley & Sons: 1992. Published online: June 1992; doi:10.1002/ffj.2730070314.

  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Fenchone&oldid=1231974814"

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    Ketones
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    Norbornanes
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