(溴甲基)环己烷
化合物
(溴甲基)环己烷是一种有机化合物，化学式为C7H13Br。它可由环己基甲醇和三溴化磷在四氢呋喃（或甲苯[1]）中反应制得。[2]它和三苯基膦在甲苯中回流，可以得到三苯基(环己基甲基)溴化鏻。[3]
| (溴甲基)环己烷 | |
|---|---|
| |
| 别名 | 溴甲基环己烷 环己基甲基溴 |
| 识别 | |
| CAS号 | 2550-36-9 
|
| PubChem | 137636 |
| SMILES |
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| 性质 | |
| 化学式 | C7H13Br |
| 摩尔质量 | 177.08 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
参考文献
- ^ Clara T. Schoeder, Anne Meyer, Andhika B. Mahardhika, Dominik Thimm, Thomas Blaschke, Mario Funke, Christa E. Müller. Development of Chromen-4-one Derivatives as (Ant)agonists for the Lipid-Activated G Protein-Coupled Receptor GPR55 with Tunable Efficacy. ACS Omega. 2019-02-28, 4 (2): 4276–4295 [2023-02-17]. ISSN 2470-1343. doi:10.1021/acsomega.8b03695. （原始内容存档于2023-02-17） （英语）.
- ^ Ying Chen, Bolin Wu, Yameng Hao, Yunqi Liu, Zhili Zhang, Chao Tian, Xianling Ning, Ying Guo, Junyi Liu, Xiaowei Wang. Structure-activity relationship studies of (E)-3,4-dihydroxystyryl alkyl sulfones as novel neuroprotective agents based on improved antioxidant, anti-inflammatory activities and BBB permeability. European Journal of Medicinal Chemistry. 2019-06, 171: 420–433 [2023-02-17]. doi:10.1016/j.ejmech.2019.03.044. （原始内容存档于2022-08-12） （英语）.
- ^ Jan Pokorný, Denisa Olejníková, Ivo Frydrych, Barbora Lišková, Soňa Gurská, Sandra Benická, Jan Šarek, Jana Kotulová, Marián Hajdúch, Petr Džubák, Milan Urban. Substituted dienes prepared from betulinic acid – Synthesis, cytotoxicity, mechanism of action, and pharmacological parameters. European Journal of Medicinal Chemistry. 2021-11, 224: 113706 [2023-02-17]. doi:10.1016/j.ejmech.2021.113706 （英语）.