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1 References  














Cadinenes






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From Wikipedia, the free encyclopedia
 


Cadinenes
α-Cadinene
α-Cadinene

α-Cadinene

β-Cadinene

γ-Cadinene

δ-Cadinene

Names
IUPAC names
  • (1S,4aR,8aR)-4,7-dimethyl-1-(propan-2-yl)- 1,2,4a,5,6,8a-hexahydronaphthalene (α-cadinene)
  • (1S,4aR,8aR)-7-methyl-4-methylidene-1-(propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene (γ-cadinene)
  • (1S,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,2,3,5,6,8a-hexahydronaphthalene (δ-cadinene)
  • Identifiers

    CAS Number

  • β: 11044-40-9 checkY
  • γ: 39029-41-9 checkY
  • δ: 1460-97-5 checkY
  • ChEBI
  • β: CHEBI:27723
  • γ: CHEBI:63203
  • δ: CHEBI:15385
  • ChEMBL
  • δ: ChEMBL445759
  • KEGG
  • β: C09625
  • γ: C19738
  • δ: C06394
  • PubChem CID

  • β: 10657
  • γ: 92313
  • δ: 441005
  • UNII
  • β: Z07LA0GY4J checkY
  • γ: 2GHT32E0JU checkY
  • δ: 7848KI47OS checkY
  • Properties

    Chemical formula

    C15H24
    Molar mass 204.357 g·mol−1

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

    checkY verify (what is checkY☒N ?)

    Infobox references

    Cadinenes are a group of isomeric hydrocarbons that occur in a wide variety of essential oil-producing plants. The name is derived from that of the Cade juniper (Juniperus oxycedrus L.), the wood of which yields an oil from which cadinene isomers were first isolated.

    Chemically, the cadinenes are bicyclic sesquiterpenes. The term cadinene has sometimes also been used in a broad sense to refer to any sesquiterpene with the so-called cadalane (4-isopropyl-1,6-dimethyldecahydronaphthalene) carbon skeleton. Because of the large number of known double-bond and stereochemical isomers, this class of compounds has been subdivided into four subclasses based on the relative stereochemistry at the isopropyl group and the two bridgehead carbon atoms.[1] The name cadinene is now properly used only for the first subclass below, which includes the compounds originally isolated from cade oil. Only one enantiomer of each subclass is depicted, with the understanding that the other enantiomer bears the same subclass name.

    References[edit]

    1. ^ A.-K. Borg-Karlson, T. Norin and A. Talvitie (1981). "Configurations and conformations of torreyol (δ-cadinol), α-cadinol, T-muurolol and T-cadinol". Tetrahedron. 37 (2): 425–430. doi:10.1016/s0040-4020(01)92031-9.

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Cadinenes&oldid=1053696737"

    Categories: 
    Flavors
    Sesquiterpenes
    Cyclohexenes
    Isopropyl compounds
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    This page was last edited on 5 November 2021, at 13:54 (UTC).

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