Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H6N2O5 |
| Molecular Weight | 198.1329 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(=C(O)C(=C1)[N+]([O-])=O)[N+]([O-])=O
InChI
InChIKey=HOYRZHJJAHRMLL-UHFFFAOYSA-N
InChI=1S/C7H6N2O5/c1-4-2-5(8(11)12)7(10)6(3-4)9(13)14/h2-3,10H,1H3
| Molecular Formula | C7H6N2O5 |
| Molecular Weight | 198.1329 |
| 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 |
|---|---|---|
| Surface functionalized mesoporous silicas as adsorbents for aromatic contaminants in aqueous solution. | 2009-07 |
|
| Solar photocatalytic degradation of 2,6-dinitro-p-cresol (DNPC) using multi-walled carbon nanotubes (MWCNTs)-TiO(2) composite photocatalysts. | 2009-05 |
|
| Lipophilic G-quadruplexes are self-assembled ion pair receptors, and the bound anion modulates the kinetic stability of these complexes. | 2003-09-10 |
|
| Hydrogen peroxide photolysis, fenton reagent and photo-fenton for the degradation of nitrophenols: a comparative study. | 2002-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:23:55 GMT 2025
by
admin
on
Mon Mar 31 22:23:55 GMT 2025
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| Record UNII |
L572BVH6NF
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| Record Status |
Validated (UNII)
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| Record Version |
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