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1 References  














Cadalene






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From Wikipedia, the free encyclopedia
 


Cadalene
Skeletal formula
Ball-and-stick model
Names
IUPAC name

4-Isopropyl-1,6-dimethylnaphthalene

Preferred IUPAC name

1,6-Dimethyl-4-(propan-2-yl)naphthalene

Other names

Cadalin

Identifiers

CAS Number

3D model (JSmol)

ChemSpider
ECHA InfoCard 100.110.415 Edit this at Wikidata

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1/C15H18/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5-10H,1-4H3

    Key: VMOJIHDTVZTGDO-UHFFFAOYAQ

  • c12c(ccc(c1ccc(c2)C)C)C(C)C

Properties

Chemical formula

C15H18
Molar mass 198.30342
Appearance Colorless liquid

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

Infobox references

Cadaleneorcadalin (4-isopropyl-1,6-dimethylnaphthalene) is a polycyclic aromatic hydrocarbon with a chemical formula C15H18 and a cadinane skeleton. It is derived from generic sesquiterpenes, and ubiquitous in essential oils of many higher plants.[1]

Cadalene, together with retene, simonellite and ip-iHMN, is a biomarkerofhigher plants, which makes it useful for paleobotanic analysis of rock sediments.

The ratio of retene to cadalene in sediments can reveal the ratio of the genus Pinaceae in the biosphere.[2]

References[edit]

  1. ^ Gomes, Alexandre de O.; Azevedo, Débora de A. (2003). "Aliphatic and aromatic hydrocarbons in tropical recent sediments of Campos dos Goytacazes, RJ, Brazil". Journal of the Brazilian Chemical Society. 14 (3): 358. doi:10.1590/S0103-50532003000300004.
  • ^ Hautevelle, Y.; Michels, R.; Malartre, F.; Trouiller, A. (2005). "Vascular plant biomarkers as ancient vegetation proxies and their stratigraphic use for tracing paleoclimatic changes during Jurassic in Western Europe" (abstract page). Geophysical Research Abstracts. 7: 10201.

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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Cadalene&oldid=1167770245"

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    This page was last edited on 29 July 2023, at 19:53 (UTC).

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