| Weight | 104.152 g/mol |
|---|---|
| Formula | C8H8 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Cyclooctatetraene (629-20-9)
1,3,5,7-cyclooctatetraene
Score:
#1525 in Physics
,
#4535 in Chemistry
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- Dibenzo[a,e]cyclooctatetraene in a proposed test for heterogeneity in catalysts formed from soluble platinum-group metal complexes (Organometallics, 1983)
- A Directly Fused Tetrameric Porphyrin Sheet and Its Anomalous Electronic Properties That Arise from the Planar Cyclooctatetraene Core (Journal of the American Chemical Society, 2006)
- Reinvestigation of the Molecular Structure of 1,3,5,7Cyclooctatetraene by Electron Diffraction (Journal of Chemical Physics, 1957)
- Transition-State Spectroscopy of Cyclooctatetraene (Science, 1996)
- Thin Films of n-Si/Poly-(CH3)3Si-Cyclooctatetraene: Conducting-Polymer Solar Cells and Layered Structures (Science, 1990)
- Lanthanide(III) complexes with cyclooctatetraene dianion. Synthetic chemistry, characterization, and physical properties (Journal of the American Chemical Society, 1973)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,3,5,7-cyclooctatetraene
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SMILESC1=CC=CC=CC=C1
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InChIKeyKDUIUFJBNGTBMD-UHFFFAOYSA-N
- Pubchem - Cyclooctatetraene
- Wikipedia - cyclooctatetraene
1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C8H8. It is also known as [8]annulene. This polyunsaturated hydrocarbon is a colorless to light yellow flammable liquid at room temperature.
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Cyclooctatetraene
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