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This is an old revision of this page, as edited by Beetstra (talk | contribs) at 17:59, 16 February 2012 (Saving copy of the {{chembox}} taken from revid 420675070 of page 3-Nitrobenzanthrone for the Chem/Drugbox validation project (updated: 'CASNo').). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 17:59, 16 February 2012 by Beetstra (talk | contribs) (Saving copy of the {{chembox}} taken from revid 420675070 of page 3-Nitrobenzanthrone for the Chem/Drugbox validation project (updated: 'CASNo').)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
This page contains a copy of the infobox ({{chembox}}) taken from revid 420675070 of page 3-Nitrobenzanthrone with values updated to verified values.
WikiProject Chemicals/Chembox validation/VerifiedDataSandbox
Names
IUPAC name 3-Nitro-3,3a-dihydro-benzoanthracen-7-one
Identifiers
3D model (JSmol)
ChemSpider
InChI
  • InChI=1S/C17H9NO3/c19-17-12-5-2-1-4-10(12)11-8-9-15(18(20)21)13-6-3-7-14(17)16(11)13/h1-9HKey: QAJOWHGESRCVLY-UHFFFAOYSA-N
  • InChI=1/C17H9NO3/c19-17-12-5-2-1-4-10(12)11-8-9-15(18(20)21)13-6-3-7-14(17)16(11)13/h1-9HKey: QAJOWHGESRCVLY-UHFFFAOYAK
SMILES
  • O=C2C1=CC=CC=C1C4=C3C2=CC=CC3C(()=O)C=C4
  • (=O)c2c1cccc4c1c(cc2)c3c(cccc3)C4=O
Properties
Chemical formula C17H9NO3
Molar mass 275.26 g/mol
Melting point 248 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Tracking categories (test):
Chemical compound
  1. Hansen, Tanja; Seidel, Albrecht; Borlak, Juergen (2007). "The environmental carcinogen 3-nitrobenzanthrone and its main metabolite 3-aminobenzanthrone enhance formation of reactive oxygen intermediates in human A549 lung epithelial cells". Toxicology and Applied Pharmacology. 221 (2): 222–234. doi:10.1016/j.taap.2007.03.003. PMID 17477947.{{cite journal}}: CS1 maint: multiple names: authors list (link)