| Weight | 113.16 g/mol |
|---|---|
| Formula | C6H11NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Cyclohexanone oxime (100-64-1)
Score:
#1361 in Physics
,
#3951 in Chemistry
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- Catalytically Active Sites for the Beckmann Rearrangement of Cyclohexanone Oxime to -Caprolactam (Journal of Catalysis, 1999)
- Hierarchically structured monolithic silicalite-1 consisting of crystallized nanoparticles and its performance in the beckmann rearrangement of cyclohexanone oxime (Journal of the American Chemical Society, 2005)
- Beckman rearrangement of cyclohexanone-oxime on HNaY zeolites: kinetic and spectroscopic studies (Applied Catalysis, 1986)
- Hydrogen Bond Driven Chemical Reactions: Beckmann Rearrangement of Cyclohexanone Oxime into -Caprolactam in Supercritical Water (Journal of the American Chemical Society, 2004)
- Active Sites of a [B]-ZSM-5 Zeolite Catalyst for the Beckmann Rearrangement of Cyclohexanone Oxime to Caprolactam (Journal of Catalysis, 2000)
- Catalytic properties of titanium silicalites: IV. Vapour phase beckmann rearrangement of cyclohexanone oxime (Journal of Catalysis, 1992)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CCC(=NO)CC1
-
InChIKeyVEZUQRBDRNJBJY-UHFFFAOYSA-N
- Pubchem - Cyclohexanone oxime
- Wikipedia - cyclohexanone oxime
Cyclohexanone oxime is an organic compound containing the functional group oxime. This colorless solid is an important intermediate in the production of nylon 6, a widely used polymer.
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Cyclohexanone oxime
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