十六烷基苯
化合物
十六烷基苯是一種有機化合物,化學式為C22H38。它可由1-十六烯和苯在催化下反應製得。[4]
十六烷基苯 | |
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別名 | 正十六烷基苯 1-苯基十六烷 |
識別 | |
CAS號 | 1459-09-2 |
PubChem | 15085 |
SMILES |
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性質 | |
化學式 | C22H38 |
摩爾質量 | 302.54 g·mol−1 |
熔點 | 27 °C[1] 26.35 °C(0.1 MPa)[2] 31.05(20 MPa)[2] |
沸點 | 230~232 °C(14 mmHg)[3] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
反應
參考文獻
- ^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFindier. [2023-11-13].
- ^ 2.0 2.1 Milhet, Michel; Pauly, Jérôme; Coutinho, João A.P.; Daridon, Jean-Luc. Solid−Liquid Equilibria under High Pressure of Nine Pure n -Alkylbenzenes. Journal of Chemical & Engineering Data. 2008-01-01, 53 (1): 233–237. ISSN 0021-9568. doi:10.1021/je700529y.
- ^ Gilman, Henry; Meals, R. N. REARRANGEMENTS IN THE FRIEDEL-CRAFTS ALKYLATION OF BENZENE. The Journal of Organic Chemistry. 1943, 08 (2): 126–146. ISSN 0022-3263. doi:10.1021/jo01190a003.
- ^ 孫學文; 趙鎖奇; 何紹群; 許志明; 張民. 以苯和丙烯為原料的烷基化反應方法. 2006. CN1785941A.
- ^ Cornely, Judith; Ham, Leyda M. Su; Meade, David E.; Dragojlovic, Veljko. Dimethyl carbonate–water: an environmentally friendly solvent system for ruthenium tetraoxide oxidations. Green Chemistry. 2003-02-11, 5 (1): 34–37. doi:10.1039/b210880c.
- ^ Bhowmik, Pradip K.; Chang, Anthony ; Kim, Jongin; Dizon, Erenz J.; Principe, Ronald Carlo G.; Han, Haesook. Thermotropic liquid-crystalline properties of viologens containing 4-n-alkylbenzenesulfonates. Crystals, 2019. 9 (2). doi:10.3390/cryst9020077.