| Weight | 112.216 g/mol |
|---|---|
| Formula | C8H16 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
CYCLOOCTANE (292-64-8)
Score:
#2202 in Physics
,
#6811 in Chemistry
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- Mechanistic Studies of the Transfer DehydrogenatiOn of Cyclooctane Catalyzed by Iridium Bis(phosphinite) p-XPCP Pincer Complexes (Journal of the American Chemical Society, 2004)
- Activation of C-H bonds in saturated hydrocarbons. The catalytic functionalisation of cyclooctane by means of some soluble iridium and ruthenium polyhydride systems (Tetrahedron Letters, 1984)
- Doped graphene as a metal-free carbocatalyst for the selective aerobic oxidation of benzylic hydrocarbons, cyclooctane and styrene. (Chemistry: A European Journal, 2013)
- Cycloheptane, cyclooctane and 1,3,5-cycloheptatriene. Low temperature thermal properties, vapor pressure and derived chemical thermodyamic properties (Journal of the American Chemical Society, 1956)
- Metallosalen complexes immobilized in zeolite NaX as catalysts of aerobic oxidation of cyclooctane (Applied Catalysis A-general, 2006)
- C-H Bond Activation by Metal Oxo Species: Chromyl Chloride Oxidations of Cyclooctane, Isobutane, and Toluene (Journal of the American Chemical Society, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CCCCCCC1
-
InChIKeyWJTCGQSWYFHTAC-UHFFFAOYSA-N
- Pubchem - CYCLOOCTANE
- Wikipedia - cyclooctane
Cyclooctane is a cycloalkane with the molecular formula (CH2)8. It is a simple colourless hydrocarbon, but it is often a reference compound for saturated eight-membered ring compounds in general.
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CYCLOOCTANE
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