Acedianthrone

Acedianthrone
Names
	Preferred IUPAC name Aceanthryleno[2,1-a]aceanthrylene-4,12-dione
Identifiers
CAS Number	129-68-0;
3D model (JSmol)	Interactive image;
ChemSpider	60550;
ECHA InfoCard	100.004.511
EC Number	204-960-3;
PubChem CID	67214;
UNII	ZTD26V6AAY ;
CompTox Dashboard (EPA)	DTXSID6059605;
	InChI InChI=1S/C30H14O2/c31-29-17-9-3-1-7-15(17)25-23-19(11-5-13-21(23)29)28-26-16-8-2-4-10-18(16)30(32)22-14-6-12-20(24(22)26)27(25)28/h1-14H Key: NUNPDAMQSBMCIG-UHFFFAOYSA-N;
	SMILES C1=CC=C2C(=C1)C3=C4C5=C6C(=CC=C5)C(=O)C7=CC=CC=C7C6=C4C8=C3C(=CC=C8)C2=O;
Properties
Chemical formula	C30H14O2
Molar mass	406.440 g·mol−1
Density	1.484 g/cm3
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Acedianthrone is an octacyclic relative of anthraquinone that is used as a pigment. It is produced from anthrone by condensation with glyoxal followed by dehydrogenation.^[2]

References

↑ Friedlander, P. H.; Goodwin, T. H.; Robertson, J. M. (1954). "Observed and calculated bond lengths in acedianthrone". Acta Crystallographica. 7: 127–128. doi:10.1107/S0365110X54000266.
↑ Bien, H.-S.; Stawitz, J.; Wunderlich, K. (2005). "Anthraquinone Dyes and Intermediates". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_355. ISBN 978-3527306732.

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[1] Friedlander, P. H.; Goodwin, T. H.; Robertson, J. M. (1954). "Observed and calculated bond lengths in acedianthrone". Acta Crystallographica. 7: 127–128. doi:10.1107/S0365110X54000266.

[UllmannDye-2] Bien, H.-S.; Stawitz, J.; Wunderlich, K. (2005). "Anthraquinone Dyes and Intermediates". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_355. ISBN 978-3527306732.

[1]

[2]