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Anthanthrene

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Anthanthrene
Skeletal formula
Ball-and-stick model of the anthanthrene molecule
Names
IUPAC name
Dibenzo[def,mno]chrysene
Other names
Anthanthren; Dibenzo[cd,jk]pyrene Hexacyclo[8.8.4.03,21.06,22.012,20.015,19]docosa-1,3,5,7,9,11,13,15,17,19,21-hendecaene[citation needed]
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.005.351 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C22H12/c1-3-13-7-9-18-12-16-6-2-4-14-8-10-17-11-15(5-1)19(13)21(18)22(17)20(14)16/h1-12H checkY
    Key: YFIJJNAKSZUOLT-UHFFFAOYSA-N checkY
  • InChI=1/C22H12/c1-3-13-7-9-18-12-16-6-2-4-14-8-10-17-11-15(5-1)19(13)21(18)22(17)20(14)16/h1-12H
    Key: YFIJJNAKSZUOLT-UHFFFAOYAI
  • c6c3ccc2cc1cccc5c1c4c2c3c(cc4cc5)cc6
Properties
C22H12
Molar mass 276.33 g/mol
Appearance Golden yellow solid
Melting point 261 °C (502 °F; 534 K)
Insoluble
-204.2·10−6 cm3/mol
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 ?)

Anthanthrene is a polycyclic aromatic hydrocarbon.[1] According to the International Agency for Research on Cancer, as of 2006 there was "limited evidence in experimental animals" that it is a carcinogen.[2]

References

  1. ^ Clar, E. (1964). Polycyclic Hydrocarbons. New York: Academic Press.
  2. ^ "PAHs: IARC Working Group, 2006". Carcinogenic Risk In Occupational Settings.


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