4-吡啶酮
4-吡啶酮 | |
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IUPAC Pyridin-4(1H)-one | |
识别 | |
CAS |
108-96-3 ![]() |
PubChem | 12290 |
ChemSpider | 11787 |
SMILES |
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InChI |
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InChIKey | GCNTZFIIOFTKIY-UHFFFAOYAB |
EINECS | 203-633-2 |
ChEBI | 133125 |
C5H5NO | |
95.1 g·mol−1 | |
无色 | |
熔点 | 150 °C(423 K) |
181 °C(454 K) | |
4-吡啶酮
5H
4NH(O),它是无色
![](https://upload.wikimedia.org/wikipedia/commons/thumb/e/e1/Fluridone.svg/232px-Fluridone.svg.png)
参考 文献 [编辑]
- ^ Weygand, Conrad. Hilgetag, G.; Martini, A. , 编. Weygand/Hilgetag Preparative Organic Chemistry 4th. New York: John Wiley & Sons, Inc. 1972: 533–534. ISBN 0471937495.
- ^ Van Allan, J. A.; Reynolds, G. A.; Alessi, J. T.; Chie Chang, S.; C. Joines, R. Reactions of 4‐pyrones with primary amines. A new class of ionic associates. Journal of Heterocyclic Chemistry. 1971, 8 (6): 919–922. doi:10.1002/jhet.5570080606.
- ^ Cook, Denys. The Preparation, Properties, and Structure of 2,6-bis-(Alkyamino)-2,5-heptadien-4-ones. Canadian Journal of Chemistry. 1963, 41 (6): 1435–1440. doi:10.1139/v63-195
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- ^ Franz Müller and Arnold P. Applebyki "Weed Control, 2. Individual Herbicides" in Ullmann's Encyclopedia of Industrial Chemistrym 2010 doi:10.1002/14356007.o28_o01
![]() | 这是 |