Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H12N2O2 |
Molecular Weight | 312.3215 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1C2=CC3=C(C=C2NC4=C1C=CC=C4)C(=O)C5=C(N3)C=CC=C5
InChI
InChIKey=NRCMAYZCPIVABH-UHFFFAOYSA-N
InChI=1S/C20H12N2O2/c23-19-11-5-1-3-7-15(11)21-17-10-14-18(9-13(17)19)22-16-8-4-2-6-12(16)20(14)24/h1-10H,(H,21,23)(H,22,24)
Approval Year
PubMed
Title | Date | PubMed |
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Acridones and quinacridones: novel fluorophores for fluorescence lifetime studies. | 2004 Mar |
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Supramolecular structures and assembly and luminescent properties of quinacridone derivatives. | 2005 Apr 28 |
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Dendritic incorporation of quinacridone: solubility, aggregation, electrochemistry, and solid-state luminescence. | 2005 Jan 28 |
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Prospective evaluation of the oxygen uptake efficiency slope as a submaximal predictor of peak oxygen uptake in aged patients with ischemic heart disease. | 2006 Aug |
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Role of lateral alkyl chains in modulation of molecular structures on metal surfaces. | 2006 Jun 9 |
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Supramolecular self-assembly initiated by solid-solid wetting. | 2007 |
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1H NMR study on the self-association of quinacridone derivatives in solution. | 2008 Nov 13 |
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Ultraviolet-visible absorption and luminescence properties of quinacridone-barium sulfate solid mixtures. | 2010 Aug |
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Sonication-induced molecular gels based on mono-cholesterol substituted quinacridone derivatives. | 2010 Feb 2 |
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Electron injection barrier reduction for organic light-emitting devices by quinacridone derivatives. | 2010 Nov 21 |
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Validation of experimental molecular crystal structures with dispersion-corrected density functional theory calculations. | 2010 Oct |
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In living color: bacterial pigments as an untapped resource in the classroom and beyond. | 2010 Oct 5 |
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CFR |
21 CFR 178.3297
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Food Contact Sustance Notif, (FCN No.) |
FCN NO. 150
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Food Contact Sustance Notif, (FCN No.) |
FCN NO. 330
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SUBSTANCE RECORD