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| Names | |
|---|---|
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Preferred IUPAC name
1,3,5-Trioxanetrione | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
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| Properties | |
| C3O6 | |
| Molar mass | 132.027 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
The chemical compound 1,3,5-trioxanetrione, or 1,3,5-trioxacyclohexane-2,4,6-trione is an unstable oxide of carbon with formula C3O6. It can be considered a cyclic trimer of carbon dioxide (CO2) or as a triple ketone of 1,3,5-trioxane (1,3,5-trioxacyclohexane). Trioxanetrione has been synthesized but is exceedingly unstable, with a half-life of approximately 40 min at −40 °C. [1] It decomposes to give carbon dioxide.
References
-
^ Rodig, Michael J.; Snow, Arthur W.; Scholl, Paul; Rea, Simon (12 June 2016).
"Synthesis and Low Temperature Spectroscopic Observation of 1,3,5-Trioxane-2,4,6-Trione: The Cyclic Trimer of Carbon Dioxide". The Journal of Organic Chemistry. 81 (13): 5354–5361.
doi:
10.1021/acs.joc.6b00647.
PMID
27183100.
 | This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it. |
|
| |
|
| |
| Names | |
|---|---|
|
Preferred IUPAC name
1,3,5-Trioxanetrione | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C3O6 | |
| Molar mass | 132.027 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
The chemical compound 1,3,5-trioxanetrione, or 1,3,5-trioxacyclohexane-2,4,6-trione is an unstable oxide of carbon with formula C3O6. It can be considered a cyclic trimer of carbon dioxide (CO2) or as a triple ketone of 1,3,5-trioxane (1,3,5-trioxacyclohexane). Trioxanetrione has been synthesized but is exceedingly unstable, with a half-life of approximately 40 min at −40 °C. [1] It decomposes to give carbon dioxide.
References
-
^ Rodig, Michael J.; Snow, Arthur W.; Scholl, Paul; Rea, Simon (12 June 2016).
"Synthesis and Low Temperature Spectroscopic Observation of 1,3,5-Trioxane-2,4,6-Trione: The Cyclic Trimer of Carbon Dioxide". The Journal of Organic Chemistry. 81 (13): 5354–5361.
doi:
10.1021/acs.joc.6b00647.
PMID
27183100.
|
| This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it. |