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Anthanthrene: Difference between revisions

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Revision as of 00:13, 12 July 2020 editMB (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers341,678 edits clean upTag: AWB← Previous edit Revision as of 20:54, 27 March 2021 edit undoLegionMammal978 (talk | contribs)Extended confirmed users7,894 editsm corrected IUPAC nameNext edit →
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| ImageSize1 = 220px | ImageSize1 = 220px
| ImageAlt1 = Ball-and-stick model of the anthanthrene molecule | ImageAlt1 = Ball-and-stick model of the anthanthrene molecule
| IUPACName = Dibenzochrysene | PIN = Naphthotetraphene
| OtherNames = Anthanthren; Dibenzopyrene | OtherNames = Dibenzochrysene; Anthanthren; Dibenzopyrene
Hexacyclodocosa-1,3,5,7,9,11,13,15,17,19,21-hendecaene{{citation needed|date=May 2019}}
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

Revision as of 20:54, 27 March 2021

Anthanthrene
Skeletal formula
Skeletal formula
Ball-and-stick model of the anthanthrene molecule
Names
Preferred IUPAC name Naphthotetraphene
Other names Dibenzochrysene; Anthanthren; Dibenzopyrene
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.005.351 Edit this at Wikidata
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • 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/h1-12HKey: YFIJJNAKSZUOLT-UHFFFAOYSA-N
  • 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/h1-12HKey: YFIJJNAKSZUOLT-UHFFFAOYAI
SMILES
  • c6c3ccc2cc1cccc5c1c4c2c3c(cc4cc5)cc6
Properties
Chemical formula C22H12
Molar mass 276.33 g/mol
Appearance Golden yellow solid
Melting point 261 °C (502 °F; 534 K)
Solubility in water Insoluble
Magnetic susceptibility (χ) -204.2·10 cm/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

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

References

  1. Clar, E. (1964). Polycyclic Hydrocarbons. New York: Academic Press.
  2. "PAHs: IARC Working Group, 2006". Carcinogenic Risk In Occupational Settings.
Polycyclic aromatic hydrocarbons
2 rings
3 rings
4 rings
5 rings
6 rings
7+ rings
General classes


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