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dc.creatorUS National Cancer Instituteen_GB
dc.date.accessioned2005-08-22T11:54:29Z
dc.date.available2005-08-22T11:54:29Z
dc.date.created2003-02-01en_GB
dc.date.issued2005-08-22T11:54:29Z
dc.identifierNSC47713en_GB
dc.identifier.urihttp://www.dspace.cam.ac.uk/handle/1810/48088
dc.format.extent6549 bytes
dc.format.mimetypechemical/x-cml
dc.language.isoen_GB
dc.publisherUnilever Center for Molecular Informatics, Cambridge Universityen_GB
dc.titleNSC47713en_GB
dc.title.alternativeAutol Red RLPen_GB
dc.title.alternativeBordeaux P51Nen_GB
dc.title.alternativeBordeaux P51Ren_GB
dc.title.alternativeC.I. Pigment Red 40en_GB
dc.title.alternativeC.I. Solvent Red 4 (8CI)en_GB
dc.title.alternativeC.I. 12170en_GB
dc.title.alternativeDainichi Naphthylamine Bordeaux 5Ben_GB
dc.title.alternativeFat Bordeauxen_GB
dc.title.alternativeFat Bordeaux Ren_GB
dc.title.alternativeGrasal Reden_GB
dc.title.alternativeLutetia Bordeaux Ben_GB
dc.title.alternativeOil Dark Reden_GB
dc.title.alternativeOil Red (VAN)en_GB
dc.title.alternativeOil Red Ben_GB
dc.title.alternativeOil Red IIRen_GB
dc.title.alternativeOil Red 2Ren_GB
dc.title.alternativeOrganol Mahogany TJen_GB
dc.title.alternativePigment Bordeauxen_GB
dc.title.alternativePigment Bordeaux Nen_GB
dc.title.alternativePigment Red RLPen_GB
dc.title.alternativePigment Red 40en_GB
dc.title.alternativeRed 2Ren_GB
dc.title.alternativeSomalia Bordeaux Ren_GB
dc.title.alternativeSudan Red 2Ren_GB
dc.title.alternativeWaxoline Red BNen_GB
dc.title.alternative1-(1-Naphthylazo)-2-naphtholen_GB
dc.title.alternative2-Naphthalenol, 1-(1-naphthalenylazo)- (9CI)en_GB
dc.typeChemical Structuresen_GB
dc.identifier.inchikeyCYZWPZHRSZNWLS-QURGRASLSA-N
dc.identifier.inchiInChI=1S/C20H14N2O/c23-19-13-12-15-7-2-4-10-17(15)20(19)22-21-18-11-5-8-14-6-1-3-9-16(14)18/h1-13,23H/b22-21+
dc.identifier.ichiC20H14N2O,23H-19-13H-12H-15-7H-2H-4H-10H-17(15)20(19)22-21-18-11H-5H-8H-14-6H-1H-3H-9H-16(14)18en_GB


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  • WWMM
    The WorldWideMolecularMatrix, an Open collection of information on small molecules

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