| Weight | 129.159 g/mol |
|---|---|
| Formula | C6H11NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
NITROCYCLOHEXANE (1122-60-7)
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- Selective hydrogenation of nitrocyclohexane to cyclohexanone oxime with h2 on decorated pt nanoparticles (Journal of Catalysis, 2009)
- Selective hydrogenation of nitrocyclohexane to cyclohexanone oxime by alumina-supported gold cluster catalysts (Journal of Molecular Catalysis A-chemical, 2011)
- Hydrogenation of nitrocyclohexane to cyclohexanone oxime over Pd/CNT catalyst under mild conditions (Catalysis Communications, 2012)
- Synthesis of polyhydroxylated -nitrocyclohexane carboxylic acids derived from D-glucose: a striking case of racemization (Tetrahedron-asymmetry, 2003)
- Gas phase hydrogenation of nitrocyclohexane over supported gold catalysts (Applied Catalysis A-general, 2013)
- Preparation, crystal structure and thermal decomposition kinetics of 1-(2,4-dinitrophenyl)azo-1-nitrocyclohexane (Journal of Molecular Structure, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CCC(CC1)[N+](=O)[O-]
-
InChIKeyNJNQUTDUIPVROZ-UHFFFAOYSA-N
- Pubchem - NITROCYCLOHEXANE
- Wikipedia - nitrocyclohexane
Nitrocyclohexane is an organic compound with the molecular formula C6H11NO2. It is listed as an extremely hazardous substance by the Emergency Planning and Community Right-to-Know Act, and the NOAA warns that it can be explosive. It is a colorless liquid, or a pale yellow liquid.
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