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1,5-Dihydroxyanthraquinone

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1,5-Dihydroxyanthraquinone
Names
Other names 1,5-dihydroxy-9,10-anthracenedione, 1,5-dihydroxyanthraquinone, Anthrarufin
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference 1881718
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.796 Edit this at Wikidata
EC Number
  • 204-175-6
Gmelin Reference 144152
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C14H8O4/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6,15-16HKey: JPICKYUTICNNNJ-UHFFFAOYSA-N
SMILES
  • C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)O
Properties
Chemical formula C14H8O4
Molar mass 240.214 g·mol
Appearance orange solid
Density 1.56 g/cm
Melting point 280 °C (536 °F; 553 K)
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
Signal word Warning
Hazard statements H315, H319, H335
Precautionary statements P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

1,5-Dihydroxyanthraquinone is an organic compound with the formula (C6H3OH)2(CO)2. It is one of several isomers of dihydroxyanthraquinone. An orange solid, it is a component of traditional Chinese medications. It serves as a chelating ligand for transition metals.

References

  1. Marasinghe, P. A. B.; Gillispie, G. D. (1993). "Structure of 1,5-dihydroxyanthraquinone: A redetermination". Acta Crystallographica Section C Crystal Structure Communications. 49 (1): 113–114. Bibcode:1993AcCrC..49..113M. doi:10.1107/s0108270192004542.
  2. "1,5-Dihydroxyanthraquinone". pubchem.ncbi.nlm.nih.gov.
  3. Cai, Yi-Zhong; Mei Sun; Jie Xing; Luo, Qiong; Corke, Harold (2006). "Structure–radical scavenging activity relationships of phenolic compounds from traditional Chinese medicinal plants". Life Sciences. 78 (25): 2872–2888. doi:10.1016/j.lfs.2005.11.004. PMID 16325868.
  4. Lin, Yue-Jian; Han, Ying-Feng; Jin, Guo-Xin (2012). "Synthesis and Structural characterization of half-sandwich iridium macro-metallacycles containing 1,5-dihydroxy-9,10- anthraquinone ligand". Journal of Organometallic Chemistry. 708–709: 31–36. doi:10.1016/j.jorganchem.2012.02.014.
Types of natural anthraquinones
Dihydroxyanthraquinones
Trihydroxyanthraquinones
Tetrahydroxyanthraquinones
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