(溴甲基)環己烷
化合物
(溴甲基)環己烷是一種有機化合物，化學式為C7H13Br。它可由環己基甲醇和三溴化磷在四氫呋喃（或甲苯[1]）中反應製得。[2]它和三苯基膦在甲苯中回流，可以得到三苯基(環己基甲基)溴化鏻。[3]
| (溴甲基)環己烷 | |
|---|---|
| |
| 別名 | 溴甲基環己烷 環己基甲基溴 |
| 識別 | |
| CAS號 | 2550-36-9 
|
| PubChem | 137636 |
| SMILES |
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| 性質 | |
| 化學式 | C7H13Br |
| 摩爾質量 | 177.08 g·mol−1 |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
參考文獻
編輯- ^ 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. （原始內容存檔於2023-02-17） （英語）.
- ^ 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. （原始內容存檔於2022-08-12） （英語）.
- ^ 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 （英語）.