Cyclooctanone
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| Identifiers | |
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3D model (
JSmol ) |
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| ChEMBL | |
| ChemSpider | |
ECHA InfoCard
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100.007.219 |
| EC Number |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C8H14O | |
| Molar mass | 126.199 g·mol−1 |
| Appearance | colorless solid |
| Melting point | 42 °C (108 °F; 315 K) |
Refractive index (nD)
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0.959 |
| Hazards | |
| GHS labelling:[1] | |
 
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| Danger | |
| H315, H319, H335 | |
| P260, P261, P264, P264+P265, P271, P280, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P319, P321, P332+P317, P337+P317, P362+P364, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cyclooctanone is an organic compound with the formula (CH2)7CO. It is a waxy white solid.
Synthesis
- It can be prepared by Jones oxidation of cyclooctanol.
- It can also be produced by ketonization reaction starting with azelaic acid.[2]
Use
Use of cyclooctanone is almost nonexistent drug chemistry with only 2 known exceptions:
See also
- Suberone
References
- ^ "Cyclooctanone". pubchem.ncbi.nlm.nih.gov.
- .
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