9-Crown-3
(Redirected from 9-crown-3)
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| Names | |
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| Preferred IUPAC name
1,4,7-Trioxonane | |
| Other names
1,4,7-Trioxacyclononane; Ethylene oxide trimer
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| 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·mol−1 |
| 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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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]
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]
See also
References
- ^ Dale, Johannes; Borgen, Gerd; Daasvatn, Kari; Liaaen-Jensen, Synnøve; Enzell, Curt R.; Mannervik, Bengt (1974). "The Oligomerization of Ethylene Oxide to Macrocyclic Ethers, Including 1,4,7-Trioxacyclononane". Acta Chemica Scandinavica. 28b: 378–379. doi:10.3891/acta.chem.scand.28b-0378.
- ^ Anderson, Wayne P.; Behm, Philip; Glennon, Timothy M.; Zerner, Michael C. (1997-03-01). "Quantum Mechanics and Molecular Mechanics Studies of the Low-Energy Conformations of 9-Crown-3". The Journal of Physical Chemistry A. 101 (10): 1920–1926. Bibcode:1997JPCA..101.1920A. doi:10.1021/jp962172h. ISSN 1089-5639.
- ^ Jagannadh, B.; Sarma, Jagarlapudi A. R. P. (1999-12-01). "Searching the Conformational Space of Cyclic Molecules: A Molecular Mechanics and Density Functional Theory Study of 9-Crown-3". The Journal of Physical Chemistry A. 103 (50): 10993–10997. Bibcode:1999JPCA..10310993J. doi:10.1021/jp991201w. ISSN 1089-5639.
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