Cyclohexanehexone
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Names | |||
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IUPAC name
cyclohexane-1,2,3,4,5,6-hexone
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Other names
hexaketocyclohexane, triquinoyl
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Identifiers | |||
3D model (
JSmol ) |
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ChemSpider | |||
ECHA InfoCard
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100.007.649 | ||
PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C6O6 | |||
Molar mass | 168.060 g·mol−1 | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cyclohexanehexone, also known as hexaketocyclohexane and triquinoyl, is an organic compound with formula C6O6, the sixfold ketone of cyclohexane. It is an oxide of carbon (an oxocarbon), a hexamer of carbon monoxide.
The compound is expected to be highly unstable, even less stable than the cyclohexanehexathione analog, and as of 1999 had only been observed as an ionized fragment during mass spectrometry studies.[1][2]
Related compounds
Cyclohexanehexone can be viewed as the neutral counterpart of the
According to
In 1966, Howard E. Worne of Natick Chemical Industries patented compounds with formulas C10O8 and C14O10, which can be described as the fusion of two or three molecules of C6O6, claimed to be produced by the action of
Triquinoyl therapy
In the late 1940s, William J. Hale claimed that "triquinoyl", being a
See also
- Cyclopentanepentone
- Ethylenetetracarboxylic dianhydride, an isomer of C6O6.
- Cyclohexanehexathione, with same structure but with sulfur instead of oxygen.
References
- ^ Gunther Seitz; Peter Imming (1992). "Oxocarbons and pseudooxocarbons". Chemical Reviews. 92 (6): 1227–1260. .
- ISSN 1387-3806.
- PMID 17044687.
- ^ .
- ISSN 0022-3654.
- ^ US 3227641, Worne, Howard E., "Polycarbonyls", issued 1996-01-04, assigned to Natick Chemical Industries
- ^ Hale, William J. (1949). "Farmer Victorious—Money, Mart, and Mother Earth" (reprint).[permanent dead link]
- ^ Goodrich, William W. (October 15–16, 1986). "FDA Oral History Interview, Goodrich" (PDF) (Interview). Interviewed by Ronald T. Ottes and Fred L. Lofsvold. p. 31.
- ^ "Import Alert #66-46 – Unapproved Version of Rodaquin". U. S. Food and Drug Administration. 1989. Archived from the original on 2016-11-16. Retrieved 2019-03-09.