| Weight | 107.112 g/mol |
|---|---|
| Formula | C6H5NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
NITROSOBENZENE (586-96-9)
nitrosobenzene, 14C-labeled
Score:
#2153 in Physics
,
#6678 in Chemistry
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LabBot
- Catalytic enantioselective synthesis of -aminooxy and -hydroxy ketone using nitrosobenzene (Journal of the American Chemical Society, 2003)
- Addition, Reduction, and Oxidation Reactions of Nitrosobenzene (Chemical Reviews, 1994)
- Reactions of nitrosobenzene with reduced glutathione (Chemico-Biological Interactions, 1979)
- The Role of the Mars and Van Krevelen Mechanism in the Selective Oxidation of Nitrosobenzene and the Deoxygenation of Nitrobenzene on Oxidic Catalysts (Journal of Catalysis, 1995)
- Electrochemical reactions of organic compounds in liquid ammonia. II. Nitrobenzene and nitrosobenzene (Journal of the American Chemical Society, 1975)
- Reactions of resonance stabilized anions. XXIX. Electron-transfer processes. 7. Formation of paramagnetic and condensation products from nitrosobenzene in basic solution (Journal of the American Chemical Society, 1967)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - nitrosobenzene, 14C-labeled
-
SMILESC1=CC=C(C=C1)N=O
-
InChIKeyNLRKCXQQSUWLCH-UHFFFAOYSA-N
- Pubchem - NITROSOBENZENE
- Wikipedia - nitrosobenzene
Nitrosobenzene is the organic compound with the formula C6H5NO. This diamagnetic species exists in equilibrium with its dimer.
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