Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H16N2 |
| Molecular Weight | 296.3651 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N1C(=NC(=C1C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4
InChI
InChIKey=RNIPJYFZGXJSDD-UHFFFAOYSA-N
InChI=1S/C21H16N2/c1-4-10-16(11-5-1)19-20(17-12-6-2-7-13-17)23-21(22-19)18-14-8-3-9-15-18/h1-15H,(H,22,23)
| Molecular Formula | C21H16N2 |
| Molecular Weight | 296.3651 |
| 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 |
|---|---|---|
| 4-[4,5-Bis(pyridin-2-yl)-1H-imidazol-2-yl]phenol monohydrate. | 2010-12-18 |
|
| Activation parameters for the recombination reaction of intramolecular radical pairs generated from the radical diffusion-inhibited HABI derivative. | 2008-07-10 |
|
| Organic nanocrystals with tunable morphologies and optical properties prepared through a sonication technique. | 2006-07-28 |
|
| Lophine derivatives as versatile analytical tools. | 2003-04-30 |
|
| Synthesis of fluorescent diarylethenes having a 2,4,5-triphenylimidazole chromophore. | 2001-08-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:42:50 GMT 2025
by
admin
on
Mon Mar 31 19:42:50 GMT 2025
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| Record UNII |
Q6K46G80ZD
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| Record Status |
Validated (UNII)
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| Record Version |
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