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(溴甲基)环己烷

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(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  checkY
PubChem 137636
SMILES
 
  • C1CCCCC1CBr
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。

(溴甲基)环己烷是一种有机化合物,化学式为C7H13Br。它可由环己基甲醇三溴化磷四氢呋喃(或甲苯[1])中反应制得。[2]它和三苯基膦甲苯中回流,可以得到三苯基(环己基甲基)溴化鏻。[3]

参考文献

  1. ^ 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). 
  2. ^ 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). 
  3. ^ 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).