5-癸酮
化合物
5-癸酮（英語：5-decanone）是一種有機化合物，化學式C10H20O，可見於石榴[2]等物種。它可由5-癸醇在催化下氧化製得[3]，或由己酰氯和正丁基氯化鎂（或正丁基鋰[4]）反應得到。[5]
| 5-癸酮 | |
|---|---|
| |
| 英文名 | 5-decanone |
| 識別 | |
| CAS號 | 820-29-1 
|
| PubChem | 13175 |
| SMILES |
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| InChI |
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| InChIKey | JDPQWHLMBJZURR-UHFFFAOYSA-N |
| 性質 | |
| 化學式 | C10H20 |
| 摩爾質量 | 140.27 g·mol−1 |
| 沸點 | 84—86 °C（357—359 K）（8 mmHg）[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
參考資料
編輯- ^ G. Forrest Woods; Henry F. Lederle. The Chemistry of Pentadienal and its Derivatives. J. Am. Chem. Soc. 1951, 73, 5, 2245–2247. doi:10.1021/ja01149a093.
- ^ A.M.M. Costa; L.O. Silva. Chemical composition of commercial cold-pressed pomegranate (Punica granatum) seed oil from Turkey and Israel, and the use of bioactive compounds for samples’ origin preliminary discrimination. Journal of Food Composition and Analysis. 2018-09, 75. doi:10.1016/J.JFCA.2018.09.004.
- ^ Park, Kwihwan; Jiang, Jing; Yamada, Tsuyoshi; Sajiki, Hironao. Ruthenium-on-carbon-catalyzed facile solvent-free oxidation of alcohols: efficient progress under solid-solid (liquid)-gas conditions. Source Chemical & Pharmaceutical Bulletin, 2021. 69 (12): 1200-1205. doi:10.1248/cpb.c21-00749.
- ^ Jae Kyo Park , Won Kyu Shin , Duk Keun An. An effective one-pot conversion of acid chlorides to aldehydes and ketones. Tetrahedron Letters, 2013. 54 (24): 3199-3203. doi:10.1016/j.tetlet.2013.04.041.
- ^ Maria Michela Dell'Anna; Piero Mastrorilli, Cosimo F Nobile, Giuseppe Marchese, Maria Rosaria Taurino. Coupling reactions between acyl chlorides and Grignard reagents in the presence of a supported Fe(III)-complex. Journal of Molecular Catalysis A: Chemical, 2000. 161 (1-2): 239-243. doi:10.1016/S1381-1169(00)00268-5.
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