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)
Molecular Formula | C20H12N2O2 |
Molecular Weight | 312.3215 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Early stages of particle formation in precipitation reactions-quinacridone and boehmite as generic examples. | 2003 Mar 1 |
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Contact dermatitis from red tattoo pigment (quinacridone) with secondary spread. | 2003 Nov |
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Monodispersed quinacridone nanocrystals prepared by a high-temperature and high-pressure liquid crystallization method. | 2003 Oct |
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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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STM study on quinacridone derivative assemblies: modulation of the two-dimensional structure by coadsorption with dicarboxylic acids. | 2005 Aug 2 |
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Dendritic incorporation of quinacridone: solubility, aggregation, electrochemistry, and solid-state luminescence. | 2005 Jan 28 |
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Preferential interactions in pigmented, polymer blends - C.I. Pigment Blue 15:4 and C.I. Pigment Red 122 - as used in a poly(carbonate)-poly(butylene terephthalate) polymer blend. | 2005 Nov 18 |
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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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Disodium 2,5-bis(phenylamino)terephthalate decahydrate, an intermediate in the industrial synthesis of quinacridone pigments. | 2006 Feb |
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Role of lateral alkyl chains in modulation of molecular structures on metal surfaces. | 2006 Jun 9 |
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Solution and solid-state spectra of quinacridone derivatives as viewed from the intermolecular hydrogen bond. | 2006 Oct 5 |
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The pi-pi stacked geometries and association thermodynamics of quinacridone derivatives studied by 1H NMR. | 2006 Sep 21 |
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Supramolecular self-assembly initiated by solid-solid wetting. | 2007 |
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Rietveld refinement of a wrong crystal structure. | 2007 Dec |
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STM study on 2D molecular assemblies of luminescent quinacridone derivatives: structure fine-tuned by introducing bulky substitutes and co-adsorption with monofunctional/bifunctional acid. | 2007 Jan 30 |
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Alkyl and dendron substituted quinacridones: synthesis, structures, and luminescent properties. | 2007 May 17 |
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Laser fabrication and spectroscopy of organic nanoparticles. | 2008 Dec |
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1H NMR study on the self-association of quinacridone derivatives in solution. | 2008 Nov 13 |
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Theoretical analysis of the intermolecular interaction effects on the excitation energy of organic pigments: solid state quinacridone. | 2008 Oct 30 |
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Alkyl chain length dependent morphology and emission properties of the organic micromaterials based on fluorinated quinacridone derivatives. | 2009 Mar 3 |
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Inadvertent polychlorinated biphenyls in commercial paint pigments. | 2010 Apr 15 |
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Ultraviolet-visible absorption and luminescence properties of quinacridone-barium sulfate solid mixtures. | 2010 Aug |
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Direct observation of enantiospecific substitution in a two-dimensional chiral phase transition. | 2010 Aug 4 |
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Sonication-induced molecular gels based on mono-cholesterol substituted quinacridone derivatives. | 2010 Feb 2 |
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Anchoring of a single molecular rotor and its array on metal surfaces using molecular design and self-assembly. | 2010 Feb 9 |
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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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Quinacridone-based molecular donors for solution processed bulk-heterojunction organic solar cells. | 2010 Sep |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:34:16 GMT 2023
by
admin
on
Fri Dec 15 15:34:16 GMT 2023
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Record UNII |
11P487375P
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Record Status |
Validated (UNII)
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Record Version |
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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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