9-Crown-3
Chemical compound
From Wikipedia, the free encyclopedia
9-Crown-3, also called 1,4,7-trioxonane or 1,4,7-trioxacyclononane, is a crown ether with the formula (C2H4O)3. A colorless liquid, it is obtained in low yield by the acid-catalyzed oligomerization of ethylene oxide.[1]
| Names | |
|---|---|
| Preferred IUPAC name
1,4,7-Trioxonane | |
| Other names
1,4,7-Trioxacyclononane; Ethylene oxide trimer | |
| Identifiers | |
3D model (JSmol) |
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| 1421638 | |
| ChEBI | |
| ChemSpider | |
PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| C6H12O3 | |
| Molar mass | 132.159 g·molâ1 |
| Appearance | Colorless liquid |
| Melting point | 0 °C (32 °F; 273 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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In contrast to larger crown ethers (12-crown-4, and 18-crown-6), 9-crown-3 has elicited very little interest, except from theorists.[2][3]
