环癸烯

环癸烯（化学式：C₁₀H₁₈）是十个碳的环烯烃。

环癸烯
IUPAC名 (E)-Cyclodecene, (Z)-Cyclodecene
别名	cis-Cyclodecene, trans-Cyclodecene
识别
CAS号	3618-12-0 ^Y 2198-20-1（E） ^Y 935-31-9（Z） ^Y
ChemSpider	4517575
SMILES	C\1=C\CCCCCCCC/1
性质
化学式	C10H18
摩尔质量	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]
沸点	143—144 °C（416—417 K）^[1] 198—199 °C（471—472 K）^[3] 194—195 °C（467—468 K）^[4]
若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

性质

环癸烯具有烯烃的通性，如可以发生臭氧化反应^[5]、和卤素的加成反应^[6][7]、环氧化反应^[8]等。

参见

• 癸烷
• 癸烯
• 环癸五烯
• 环癸烷

参考文献

1. Willstatter, Richard; Veraguth, Hans. Cyclooctane Series. II. Communication. Berichte der Deutschen Chemischen Gesellschaft, 1907. 40. 959-970. ISSN: 0365-9496.
2. Schenker, Prelog, K.; Gunthard, H. H. Carbon rings. LX. The ten-membered ring. V. Helvetica Chimica Acta, 1952. 35: 1598-1615. ISSN: 0018-019X.
3. 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 （英语）. 
4. 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. （原始内容于2019-12-30） （英语）. 
5. 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 （英语）. 
6. 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.
7. 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.
8. 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 （英语）.