| Weight | 198.225 g/mol |
|---|---|
| Formula | C12H10N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
AZOXYBENZENE
fenazox · fenazox, (Z)-isomer · fenazox, (E)-isomer
20972-43-4, 21650-65-7, 495-48-7
Score:
#1390 in Physics
,
#4054 in Chemistry
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- 3,4,3',4'-Tetrachloro azoxybenzene and azobenzene: potent inducers of aryl hydrocarbon hydroxylase (Science, 1976)
- Nematic and cholesteric thermotropic polyesters with azoxybenzene mesogenic units and flexible spacers in the main chain (Journal of Polymer Science Part B, 1982)
- TS-1 oxidation of aniline to azoxybenzene in a microstructured reactor (Applied Catalysis A-general, 2005)
- The efficient electrochemical reduction of nitrobenzene and azoxybenzene to aniline in neutral and basic aqueous methanolic solutions at devarda copper and raney nickel electrodes: electrocatalytic hydrogenolysis of NO and NN bonds (Electrochimica Acta, 1990)
- Dielectric Properties of Di-n-Heptyl Azoxybenzene in the Nematic and in the Smectic-APhases (Physical Review Letters, 1974)
- The electrochemical reduction of nitrobenzene and azoxybenzene in neutral and basic aqueous methanolic solutions at polycrystalline copper and nickel electrodes (Electrochimica Acta, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - fenazox
- fenazox, (Z)-isomer
- fenazox, (E)-isomer
-
SMILESC1=CC=C(C=C1)N=[N+](C2=CC=CC=C2)[O-]
-
InChIKeyGAUZCKBSTZFWCT-UHFFFAOYSA-N
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