4-Piridon
4-Piridon je organsko jedinjenje sa formulom C
5H
4NH(O).
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| Identifikacija | |
|---|---|
3D model (Jmol)
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.003.304 |
| EC broj | 203-633-2 |
| UNII | |
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| Svojstva | |
| C5H5NO | |
| Molarna masa | 95,10 g·mol−1 |
| Tačka topljenja | 150°C |
| Tačka ključanja | 181°C |
| Rastvoran u vodi | |
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
| Reference infokutije | |
Priprema уреди
4-Piridon, i njegovi derivati, se pripremaju iz 4-Pirona i amina u protičnim rastvaračima.[3][4][5]
Vidi još уреди
Reference уреди
- ^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- ^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
- ^ Weygand, Conrad (1972). Hilgetag, G.; Martini, A., ур. Weygand/Hilgetag Preparative Organic Chemistry (4th изд.). New York: John Wiley & Sons, Inc. стр. 533-534. ISBN 0471937495.
- ^ Van Allan, J. A.; Reynolds, G. A.; Alessi, J. T.; Chie Chang, S.; C. Joines, R. (1971). „Reactions of 4‐pyrones with primary amines. A new class of ionic associates”. Journal of Heterocyclic Chemistry. 8 (6): 919—922. doi:10.1002/jhet.5570080606.
- ^ Cook, Denys (1963). „The Preparation, Properties, and Structure of 2,6-bis-(Alkyamino)-2,5-heptadien-4-ones”. Canadian Journal of Chemistry. 41 (6): 1435—1440. doi:10.1139/v63-195.