Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H6N2O2 |
| Molecular Weight | 174.1561 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[O-][N+](=O)C1=CC=CC2=C1N=CC=C2
InChI
InChIKey=OQHHSGRZCKGLCY-UHFFFAOYSA-N
InChI=1S/C9H6N2O2/c12-11(13)8-5-1-3-7-4-2-6-10-9(7)8/h1-6H
| Molecular Formula | C9H6N2O2 |
| Molecular Weight | 174.1561 |
| 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 |
|---|---|---|
| Fragmentation mechanisms in electron ionization mass spectrometry of 5-nitro- and 8-nitroquinoline: a comparative study. | 2008 |
|
| Ring-substituted quinolines as potential anti-tuberculosis agents. | 2004-05-15 |
|
| [Formations and reactions of aromatic furazan compounds]. | 2001-06 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:34:39 GMT 2025
by
admin
on
Mon Mar 31 18:34:39 GMT 2025
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| Record UNII |
YWO6S88V4V
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| Record Status |
Validated (UNII)
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| Record Version |
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