Back أكسازوليدين Arabic اوکسازولیدین AZB Oxazolidin German Oksazolidino Esperanto اوکسازولیدین Persian Oxazolidine French Ossazolidina Italian オキサゾリジン Japanese Oxazolidine Dutch Oksazolidyna Polish
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| Names | |
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| Preferred IUPAC name
1,3-Oxazolidine[1] | |
| Other names
Oxazolidine
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.127.875 |
| MeSH | C064210 |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C3H7NO | |
| Molar mass | 73.0938 g/mol |
| Appearance | colorless liquid |
| Density | 1.063 g/mL |
| Melting point | 90 °C (194 °F; 363 K) |
| Boiling point | 200 °C (392 °F; 473 K) 20 torr |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Oxazolidine is a five-membered heterocycle ringwith the formula (CH2)3(NH)O.The O atom and NH groups are not mutually bonded, in contrast to isoxazolidine.[2][3] Oxazolidines (emphasis on plural) are derivatives of the parent oxazolidine owing to the presence of substituents on carbon and/or nitrogen. Oxazolines are unsaturated analogues of oxazolidines.
- ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 142. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
- ^ "SID 3881507 -- PubChem Substance Summary". The PubChem Project. United States National Center for Biotechnology Information. Retrieved 13 December 2005.
- ^ Cordero, Franca M.; Giomi, Donatella; Lascialfari, Luisa (2013). Five-Membered Ring Systems. Progress in Heterocyclic Chemistry. Vol. 25. pp. 291–317. doi:10.1016/B978-0-08-099406-2.00012-1. ISBN 978-0-08-099406-2.