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1047-16-1 | Quinolino[2,3-b]acridine-7,14(5H,12H);-dione
CAS No: 1047-16-1 Catalog No: AG003U3C MDL No:MFCD00059956
Product Description
Catalog Number:
AG003U3C
Chemical Name:
Quinolino[2,3-b]acridine-7,14(5H,12H);-dione
CAS Number:
1047-16-1
Molecular Formula:
C20H12N2O2
Molecular Weight:
312.3215
MDL Number:
MFCD00059956
IUPAC Name:
5,12-dihydroquinolino[2,3-b]acridine-7,14-dione
InChI:
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)
InChI Key:
NRCMAYZCPIVABH-UHFFFAOYSA-N
SMILES:
O=c1c2cc3[nH]c4ccccc4c(=O)c3cc2[nH]c2c1cccc2
EC Number:
213-879-2
UNII:
11P487375P
NSC Number:
316165
Properties
Complexity:
500
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
312.09g/mol
Formal Charge:
0
Heavy Atom Count:
24
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
312.328g/mol
Monoisotopic Mass:
312.09g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
58.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4
Literature
| Title | Journal |
|---|---|
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| Fabrication of the smallest organic nanocolloids by a top-down method based on laser ablation. | Chemical record (New York, N.Y.) 20110201 |
| Attenuation of cytotoxic natural product DNA intercalating agents by caffeine. | Scientia pharmaceutica 20110101 |
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| In living color: bacterial pigments as an untapped resource in the classroom and beyond. | PLoS biology 20101001 |
| Quinacridone-based molecular donors for solution processed bulk-heterojunction organic solar cells. | ACS applied materials & interfaces 20100901 |
| Direct observation of enantiospecific substitution in a two-dimensional chiral phase transition. | Journal of the American Chemical Society 20100804 |
| Ultraviolet-visible absorption and luminescence properties of quinacridone-barium sulfate solid mixtures. | Applied spectroscopy 20100801 |
| Inadvertent polychlorinated biphenyls in commercial paint pigments. | Environmental science & technology 20100415 |
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| Anchoring of a single molecular rotor and its array on metal surfaces using molecular design and self-assembly. | International journal of molecular sciences 20100101 |
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| Laser fabrication and spectroscopy of organic nanoparticles. | Accounts of chemical research 20081201 |
| 1H NMR study on the self-association of quinacridone derivatives in solution. | The journal of physical chemistry. A 20081113 |
| Theoretical analysis of the intermolecular interaction effects on the excitation energy of organic pigments: solid state quinacridone. | The journal of physical chemistry. A 20081030 |
| Rietveld refinement of a wrong crystal structure. | Acta crystallographica. Section B, Structural science 20071201 |
| Alkyl and dendron substituted quinacridones: synthesis, structures, and luminescent properties. | The journal of physical chemistry. B 20070517 |
| STM study on 2D molecular assemblies of luminescent quinacridone derivatives: structure fine-tuned by introducing bulky substitutes and co-adsorption with monofunctional/bifunctional acid. | Langmuir : the ACS journal of surfaces and colloids 20070130 |
| Supramolecular self-assembly initiated by solid-solid wetting. | Chemistry (Weinheim an der Bergstrasse, Germany) 20070101 |
| Solution and solid-state spectra of quinacridone derivatives as viewed from the intermolecular hydrogen bond. | The journal of physical chemistry. B 20061005 |
| The pi-pi stacked geometries and association thermodynamics of quinacridone derivatives studied by 1H NMR. | The journal of physical chemistry. A 20060921 |
| Prospective evaluation of the oxygen uptake efficiency slope as a submaximal predictor of peak oxygen uptake in aged patients with ischemic heart disease. | American heart journal 20060801 |
| Role of lateral alkyl chains in modulation of molecular structures on metal surfaces. | Physical review letters 20060609 |
| Disodium 2,5-bis(phenylamino)terephthalate decahydrate, an intermediate in the industrial synthesis of quinacridone pigments. | Acta crystallographica. Section C, Crystal structure communications 20060201 |
| 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. | Journal of chromatography. A 20051118 |
| STM study on quinacridone derivative assemblies: modulation of the two-dimensional structure by coadsorption with dicarboxylic acids. | Langmuir : the ACS journal of surfaces and colloids 20050802 |
| Supramolecular structures and assembly and luminescent properties of quinacridone derivatives. | The journal of physical chemistry. B 20050428 |
| Dendritic incorporation of quinacridone: solubility, aggregation, electrochemistry, and solid-state luminescence. | Chemical communications (Cambridge, England) 20050128 |
| Acridones and quinacridones: novel fluorophores for fluorescence lifetime studies. | Journal of fluorescence 20040301 |
| Contact dermatitis from red tattoo pigment (quinacridone) with secondary spread. | Contact dermatitis 20031101 |
| Monodispersed quinacridone nanocrystals prepared by a high-temperature and high-pressure liquid crystallization method. | Journal of nanoscience and nanotechnology 20031001 |
| Early stages of particle formation in precipitation reactions-quinacridone and boehmite as generic examples. | Journal of colloid and interface science 20030301 |
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