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Contents

   



(Top)
 


1 See also  





2 References  














Cedrene






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From Wikipedia, the free encyclopedia
 


(−)-α-cedrene
Names
IUPAC name

Cedr-8-ene

Systematic IUPAC name

(3R,3aS,7S,8aS)-3,6,8,8-Tetramethyl-2,3,4,7,8,8a-hexahydro-1H-3a,7-methanoazulene

Identifiers

CAS Number

  • 469-61-4 (α) checkY
  • 546-28-1 (β) checkY
  • 3D model (JSmol)

    Beilstein Reference

    2207578
    ChEBI
    ChemSpider
    ECHA InfoCard 100.031.131 Edit this at Wikidata
    EC Number
    • 234-257-7
    KEGG

    PubChem CID

    UNII
  • 50D4A81G8T (α) checkY
  • 6QL7ERD5Q1 (β) checkY
    • InChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H3/t11-,12+,13+,15+/m1/s1

      Key: IRAQOCYXUMOFCW-OSFYFWSMSA-N

    • InChI=1/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H3/t11-,12+,13+,15+/m1/s1

      Key: IRAQOCYXUMOFCW-OSFYFWSMBF

    • C[C@@H]1CC[C@@H]2[C@]13CC=C([C@H](C3)C2(C)C)C

    Properties

    Chemical formula

    C15H24
    Molar mass 204.357 g·mol−1
    Density 0.932 g/mL at 20 °C[1]
    Boiling point 261–262 °C[1]
    Hazards
    GHS labelling:

    Pictograms

    GHS02: FlammableGHS08: Health hazardGHS09: Environmental hazard

    Signal word

    Danger

    Hazard statements

    H226, H304, H410

    Precautionary statements

    P210, P233, P240, P241, P242, P243, P273, P280, P301+P310, P303+P361+P353, P331, P370+P378, P391, P403+P235, P405, P501

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

    Infobox references

    (+)-β-cedrene
    Names
    IUPAC name

    Cedr-8(15)-ene

    Systematic IUPAC name

    (3R,3aS,7S,8aS)-3,6,8,8-Tetramethyl-6-methylideneoctahydro-1H-3a,7-methanoazulene

    Identifiers

    CAS Number

    3D model (JSmol)

    ChemSpider
    ECHA InfoCard 100.031.131 Edit this at Wikidata

    PubChem CID

    UNII
    • InChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h11-13H,1,5-9H2,2-4H3/t11-,12+,13+,15+/m1/s1

      Key: DYLPEFGBWGEFBB-OSFYFWSMSA-N

    • InChI=1/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h11-13H,1,5-9H2,2-4H3/t11-,12+,13+,15+/m1/s1

      Key: DYLPEFGBWGEFBB-OSFYFWSMBA

    • C[C@@H]1CC[C@@H]2[C@]13CCC(=C)[C@H](C3)C2(C)C

    Properties

    Chemical formula

    C15H24
    Molar mass 204.357 g·mol−1
    Density 0.932 g/mL at 20 °C[2]
    Boiling point 263–264 °C[2]

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

    Infobox references

    Cedrene is a sesquiterpene found in the essential oilofcedar. The two isomers present in the oil are (−)-α-cedrene[3][4] and (+)-β-cedrene,[5] which differ in the position of a double bond.

    See also[edit]

    References[edit]

    1. ^ a b Sigma-Aldrich Co., (−)-α-Cedrene. Retrieved on 8 July 2012.
  • ^ a b Sigma-Aldrich Co., (+)-β-Cedrene. Retrieved on 8 July 2012.
  • ^ Lee, H. Y.; Lee, S.; Kim, D.; Kim, B. K.; Bahn, J. S.; Kim, S. (1998). "Total synthesis of α-cedrene: A new strategy utilizing N-aziridinylimine radical chemistry". Tetrahedron Letters. 39 (42): 7713–7716. doi:10.1016/S0040-4039(98)01680-3.
  • ^ Takigawa, H.; Kubota, H.; Sonohara, H.; Okuda, M.; Tanaka, S.; Fujikura, Y.; Ito, S. (1993). "Novel allylic oxidation of α-cedrene to sec-cedrenol by a Rhodococcus strain". Applied and Environmental Microbiology. 59 (5): 1336–1341. Bibcode:1993ApEnM..59.1336T. doi:10.1128/aem.59.5.1336-1341.1993. PMC 182086. PMID 16348930.
  • ^ Kerr, W. J.; McLaughlin, M.; Morrison, A. J.; Pauson, P. L. (2001). "Formal total synthesis of (±)-α- and β-cedrene by preparation of cedrone. Construction of the tricyclic carbon skeleton by the use of a highly efficient intramolecular Khand annulation". Organic Letters. 3 (19): 2945–2948. doi:10.1021/ol016054a. PMID 11554814.
  • t
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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Cedrene&oldid=1223933514"

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