Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H10N2O2 |
| Molecular Weight | 238.2414 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC2=C(C=C1)C(=O)C3=CC(N)=CC=C3C2=O
InChI
InChIKey=WQOWBWVMZPPPGX-UHFFFAOYSA-N
InChI=1S/C14H10N2O2/c15-7-1-3-9-11(5-7)14(18)10-4-2-8(16)6-12(10)13(9)17/h1-6H,15-16H2
| Molecular Formula | C14H10N2O2 |
| Molecular Weight | 238.2414 |
| 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 |
|---|---|---|
| Study of preferential solvation of 2,6-diaminoanthraquinone in binary mixtures by absorption and fluorescence studies. | 2008-08 |
|
| Solvent polarity induced structural changes in 2,6-diamino-9,10-anthraquinone dye. | 2008-01 |
|
| Photophysical behaviour of 2,6-diaminoanthraquinone in different solvents and at various pH. | 2007-11 |
|
| Long-wavelength analogue of PRODAN: synthesis and properties of Anthradan, a fluorophore with a 2,6-donor-acceptor anthracene structure. | 2006-12-22 |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005-06 |
|
| A homogeneous time-resolved fluorescence detection of telomerase activity. | 2004-10-01 |
|
| Nanowells on silica particles in water containing long-distance porphyrin heterodimers. | 2003-09-03 |
|
| Electronic absorption spectra of amino substituted anthraquinones and their interpretation using the ZINDO/S and AM1 methods. | 2003-05 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:30:44 GMT 2025
by
admin
on
Mon Mar 31 19:30:44 GMT 2025
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| Record UNII |
3DY0EUZ2ZM
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| Record Status |
Validated (UNII)
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| Record Version |
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