Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H10N2O3S |
| Molecular Weight | 214.242 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(N=O)S(=O)(=O)C1=CC=C(C)C=C1
InChI
InChIKey=FFKZOUIEAHOBHW-UHFFFAOYSA-N
InChI=1S/C8H10N2O3S/c1-7-3-5-8(6-4-7)14(12,13)10(2)9-11/h3-6H,1-2H3
| Molecular Formula | C8H10N2O3S |
| Molecular Weight | 214.242 |
| 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 |
|---|---|---|
| Low-temperature N-O bond cleavage in nitrosyl ligands induced by the unsaturated dimolybdenum anion [Mo2(eta(5)-C5H5)2(mu-PPh2)(mu-CO)2]-. | 2009-10-05 |
|
| Transglutaminase 2 undergoes a large conformational change upon activation. | 2007-12 |
|
| Predicting the reactivity of ambidentate nucleophiles and electrophiles using a single, general-purpose, reactivity indicator. | 2007-05-21 |
|
| Kinetic model for reactivity in quaternary water-in-oil microemulsions. | 2006-11-06 |
|
| In search of fully uncomplexed cyclodextrin in the presence of micellar aggregates. | 2006-08-17 |
|
| Evidence for complexes of different stoichiometries between organic solvents and cyclodextrins. | 2006-03-21 |
|
| Reactivity of sulfur nucleophiles with N-methyl-N-nitroso-p-toluenesulfonamide. | 2004-04-21 |
|
| Basic hydrolysis of crystal violet in beta-cyclodextrin/surfactant mixed systems. | 2004-02-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:15:13 GMT 2025
by
admin
on
Mon Mar 31 19:15:13 GMT 2025
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| Record UNII |
K3089966LA
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| Record Status |
Validated (UNII)
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| Record Version |
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