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Anthanthrene: Difference between revisions

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Revision as of 17:53, 13 May 2010 editJynto (talk | contribs)Extended confirmed users3,201 edits Adding image of molecule← Previous edit Revision as of 13:39, 29 September 2010 edit undoBeetstra (talk | contribs)Edit filter managers, Administrators172,084 edits Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: ChemSpiderID InChI SMILES InChIKey.Next edit →
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| OtherNames = Anthanthren; Dibenzopyrene | OtherNames = Anthanthren; Dibenzopyrene
| Section1 = {{Chembox Identifiers | Section1 = {{Chembox Identifiers
| CASNo = 191-26-4 | ChemSpiderID = 8764
| 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
| InChIKey = YFIJJNAKSZUOLT-UHFFFAOYAI
| CASNo = 191-26-4
| CASNo_Ref = {{cascite}} | CASNo_Ref = {{cascite}}
| PubChem = | PubChem =
| SMILES = c6c3ccc2cc1cccc5c1c4c2c3c(cc4cc5)cc6
| SMILES = C12=CC=C3C(C(C(C=C6)=C5)=C(C6=CC=C4)C4=C3)=C1C5=CC=C2
}} }}
| Section2 = {{Chembox Properties | Section2 = {{Chembox Properties
| Formula = C<sub>22</sub>H<sub>12</sub> | Formula = C<sub>22</sub>H<sub>12</sub>

Revision as of 13:39, 29 September 2010

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Anthanthrene
Skeletal formula
Skeletal formula
Ball-and-stick model
Ball-and-stick model
Names
IUPAC name Dibenzochrysene
Other names Anthanthren; Dibenzopyrene
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.005.351 Edit this at Wikidata
CompTox Dashboard (EPA)
InChI
  • 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
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Anthanthrene is a polycyclic aromatic hydrocarbon.


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References

  1. Clar, E. (1964). Polycyclic Hydrocarbons. New York: Academic Press.
Polycyclic aromatic hydrocarbons
2 rings
3 rings
4 rings
5 rings
6 rings
7+ rings
General classes
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