環癸烯
外觀
環癸烯 | |||
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IUPAC名 (E)-Cyclodecene, (Z)-Cyclodecene | |||
別名 | cis-Cyclodecene, trans-Cyclodecene | ||
識別 | |||
CAS號 | 3618-12-0 ![]() 2198-20-1(E) ![]() 935-31-9(Z) ![]() | ||
ChemSpider | 4517575 | ||
SMILES |
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性質 | |||
化學式 | C10H18 | ||
摩爾質量 | 138.25 g·mol−1 | ||
密度 | 0.887 g/cm−3(0 °C)[1] 0.8681 g/cm−3(E, 20 °C)[2] 0.8743 g/cm−3(Z, 20 °C)[2] | ||
沸點 | 143—144 °C(416—417 K)[1] 198—199 °C(471—472 K)[3] 194—195 °C(467—468 K)[4] | ||
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
性質
[編輯]環癸烯具有烯烴的通性,如可以發生臭氧化反應[5]、和鹵素的加成反應[6][7]、環氧化反應[8]等。
參見
[編輯]參考文獻
[編輯]- ^ 1.0 1.1 Willstatter, Richard; Veraguth, Hans. Cyclooctane Series. II. Communication. Berichte der Deutschen Chemischen Gesellschaft, 1907. 40. 959-970. ISSN: 0365-9496.
- ^ 2.0 2.1 Schenker, Prelog, K.; Gunthard, H. H. Carbon rings. LX. The ten-membered ring. V. Helvetica Chimica Acta, 1952. 35: 1598-1615. ISSN: 0018-019X.
- ^ Richard B. Turner, W. R. Meador. Heats of Hydrogenation. IV. Hydrogenation of Some cis- and trans-Cycloölefins 1. Journal of the American Chemical Society. 1957-08, 79 (15): 4133–4136 [2020-05-02]. ISSN 0002-7863. doi:10.1021/ja01572a042 (英語).
- ^ A. T. Blomquist, Robert E. Burge, Arthur C. Sucsy. Many-Membered Carbon Rings. V. Cyclodecyne, cis- and trans-Cyclodecene and Related Compounds 1. Journal of the American Chemical Society. 1952-07, 74 (14): 3636–3642 [2020-05-02]. ISSN 0002-7863. doi:10.1021/ja01134a051. (原始內容存檔於2019-12-30) (英語).
- ^ Karl Griesbaum, Willi Volpp, Reinhard Greinert, Hans Joachim Greunig, Juergen Schmid, Henning Henke. Ozonolysis of tetrasubstituted ethylenes, cycloolefins, and conjugated dienes on polyethylene. The Journal of Organic Chemistry. 1989-01, 54 (2): 383–389 [2020-05-02]. ISSN 0022-3263. doi:10.1021/jo00263a023 (英語).
- ^ Tarchini, Claudio; Tran Dinh An; Jan, Gerald; Schlosser, Manfred. Base-promoted elimination reactions. Part 8. Hydroxide-promoted hydrogen halide cleavage of vic-dihalides under heterogeneous conditions: reaction outcome due to surprising solvent and metal effects. Helvetica Chimica Acta, 1979. 62 (2): 635-640. ISSN: 0018-019X.
- ^ Kaushik, M. P.; Polshettiwar, Vivek. N-Octylquinolinium tribromide: a task specific quinoline based ionic liquid as a new brominating agent. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 2006. 45B (11): 2542-2545. ISSN: 0376-4699.
- ^ Tatiana R. Amarante, Patrícia Neves, Filipe A. Almeida Paz, Martyn Pillinger, Anabela A. Valente, Isabel S. Gonçalves. A dinuclear oxomolybdenum(VI) complex, [Mo2O6(4,4′-di-tert-butyl-2,2′-bipyridine)2], displaying the {MoO2(μ-O)2MoO2}0 core, and its use as a catalyst in olefin epoxidation. Inorganic Chemistry Communications. 2012-06, 20: 147–152 [2020-05-02]. doi:10.1016/j.inoche.2012.02.038 (英語).
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