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Contents

   



(Top)
 


1 Derivatives of cholestane  





2 See also  





3 References  





4 External links  














Cholestane






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This is an old revision of this page, as edited by Anselmus7 (talk | contribs)at14:48, 5 September 2017 (added further info). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
(diff)  Previous revision | Latest revision (diff) | Newer revision  (diff)

Cholestane

IUPAC numbering[1]

Names
IUPAC name

(8R,9S,10S,13R,14S,17R)-10,13-Dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene

Identifiers

CAS Number

  • 481-21-0 checkY
  • 481-20-9 checkY
  • 3D model (JSmol)

  • Interactive image
  • ChEBI
    ChemSpider
    ECHA InfoCard 100.035.496 Edit this at Wikidata

    IUPHAR/BPS

    PubChem CID

    CompTox Dashboard (EPA)

    • InChI=1S/C27H48/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h19-25H,6-18H2,1-5H3/t20-,21?,22+,23-,24+,25+,26+,27-/m1/s1 checkY

      Key: XIIAYQZJNBULGD-LDHZKLTISA-N checkY

    • InChI=1/C27H48/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h19-25H,6-18H2,1-5H3/t20-,21?,22+,23-,24+,25+,26+,27-/m1/s1

      Key: XIIAYQZJNBULGD-LDHZKLTIBN

    • C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4[C@@]3(CCCC4)C)C

    • C41CCCC[C@@]1([C@@H]3[C@H]([C@@H]2CC[C@@H]([C@@]2(C)CC3)[C@H](C)CCCC(C)C)CC4)C

    Properties

    Chemical formula

    C27H48
    Molar mass 372.681 g·mol−1
    Density 0.911 g/ml

    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

    Cholestane is a saturated 27-carbon tetracyclic triterpene. Cholestane, along with ergostane and stigmastane are used as biomarkers for early eukaryotic life[2]. High abundance of cholestane relative to the others has been interpreted as the presence of rhodophytes[3].

    Derivatives of cholestane

    Derivatives are classified in two families:

    Some steroids, such as cholesterol, are both a sterol and a cholestene.

    See also

    References

  • ^ Brocks, Jochen J.; Jarrett, Amber J. M.; Sirantoine, Eva; Hallmann, Christian; Hoshino, Yosuke; Liyanage, Tharika. "The rise of algae in Cryogenian oceans and the emergence of animals". Nature. 548 (7669): 578–581. doi:10.1038/nature23457.
  • ^ Summons, Roger E; Brassell, Simon C; Eglinton, Geoffrey; Evans, Evan; Horodyski, Robert J; Robinson, Neil; Ward, David M. "Distinctive hydrocarbon biomarkers from fossiliferous sediment of the Late Proterozoic Walcott Member, Chuar Group, Grand Canyon, Arizona". Geochimica et Cosmochimica Acta. 52 (11): 2625–2637. doi:10.1016/0016-7037(88)90031-2.
  • External links


    Retrieved from "https://en.wikipedia.org/w/index.php?title=Cholestane&oldid=799081920"

    Categories: 
    Cholestanes
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    This page was last edited on 5 September 2017, at 14:48 (UTC).

    This version of the page has been revised. Besides normal editing, the reason for revision may have been that this version contains factual inaccuracies, vandalism, or material not compatible with the Creative Commons Attribution-ShareAlike License.



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