4-Piridon
Identifikacija | |
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3D model (Jmol) |
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ChEBI |
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ChemSpider |
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ECHA InfoCard | 100.003.304 |
EC broj | 203-633-2 |
PubChem[1][2] C ID |
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UNII |
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SMILES
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Svojstva | |
C5H5NO | |
Molarna masa | 95,10 g·mol−1 |
Tačka topljenja | 150°C |
Tačka ključanja | 181°C |
Rastvorljivost u vodi | Rastvoran u vodi |
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
Reference infokutije | |
4-Piridon je organsko jedinjenje sa formulom C
5H
4NH(O).
Priprema
4-Piridon, i njegovi derivati, se pripremaju iz 4-Pirona i amina u protičnim rastvaračima.[3][4][5]
Vidi još
- 4-Piperidinon
- Dehidrosirćetna kiselina
Reference
- ^ 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. уреди
- ^ 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.