- Cyclopentanepentone
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Cyclopentanepentone Systematic nameCyclopentane-1,2,3,4,5-pentone[1]Other namesLeuconic acidIdentifiers CAS number 3617-57-0 PubChem 12305030 ChemSpider 16788087 Jmol-3D images Image 1 - O=C1C(=O)C(=O)C(=O)C1=O
Properties Molecular formula C5O5 Molar mass 140.05 g mol−1 Exact mass 139.974573110 g mol−1 (verify) (what is: / ?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Cyclopentanepentone, also known as leuconic acid, is a hypothetical organic compound with formula C5O5, the fivefold ketone of cyclopentane. It would be an oxide of carbon (an oxocarbon), indeed a pentamer of carbon monoxide.
As of 2000, the compound had yet to be synthesized in bulk, but there have been reports of trace synthesis.[2][3][4]
Related compounds
Cyclopentanepentone can be viewed as the neutral counterpart of the croconate anion C5O52−.
The compound referred to in the literature and trade as "cyclopentanepentone pentahydrate" (C5O5·5H2O) is probably decahydroxycyclopentane (C5(OH)10).[3][5]
References
- ^ "CID 12305030 - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information. http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=12305030&loc=ec_rcs.
- ^ Rubin, Mordecai B.; Gleiter, Rolf (2000). "The Chemistry of Vicinal Polycarbonyl Compounds". Chemical Reviews 100 (3): 1121. doi:10.1021/cr960079j. PMID 11749259.
- ^ a b Gunther Seitz; Peter Imming (1992). "Oxocarbons and pseudooxocarbons". Chemical Reviews 92 (6): 1227–1260. doi:10.1021/cr00014a004.
- ^ Detlef Schröder, Helmut Schwarz, Suresh Dua, Stephen J. Blanksby and John H. Bowie (1999). "Mass spectrometric studies of the oxocarbons CnOn (n = 3–6)". International Journal of Mass Spectrometry 188: 17–25. doi:10.1016/S1387-3806(98)14208-2.
- ^ Person, Willis B.; Williams, Dale G. (1957). Journal of Physical Chemistry 61 (7): 1017. doi:10.1021/j150553a047.
See also
Oxocarbons Common oxides Exotic oxides Compounds derived from oxides Categories:- Oxocarbons
- Hypothetical chemical compounds
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