二苯基溴甲烷
外觀
二苯基溴甲烷 | |
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IUPAC名 1,1′-(Bromomethylene)dibenzene | |
別名 | α-苯基苄溴 α-溴二苯甲烷 |
識別 | |
CAS號 | 776-74-9 |
PubChem | 236603 |
ChemSpider | 206530 |
SMILES |
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InChI |
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性質 | |
化學式 | C13H11Br |
摩爾質量 | 247.13 g·mol−1 |
熔點 | 45 °C(318 K)[1] |
沸點 | 178 °C(17 torr)[2] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
二苯基溴甲烷是一種有機化合物,化學式為C13H11Br。它可由二苯甲醇的溴化反應製得。[3]它和疊氮化鈉在二甲基亞碸中反應,可以得到二苯基疊氮甲烷。[4]它和甲苯在三氟化硼乙醚存在下反應,可以得到4-甲基三苯甲烷,副產物2-甲基三苯甲烷。[5]
參考文獻
[編輯]- ^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2022-3-9].
- ^ Margolis, D. S.; Pittman, R. W. Products of the interaction of hydrogen selenide and ketones. Journal of the Chemical Society, 1957: 799-805.
- ^ Nilesh R Tawari, Seema Bag, Archana Raju, Arundhati C Lele, Ranjeet Bairwa, Mukti Kanta Ray, Mgr Rajan, Laxman U Nawale, Dhiman Sarkar, Mariam S Degani. Rational drug design, synthesis and biological evaluation of dihydrofolate reductase inhibitors as antituberculosis agents. Future Medicinal Chemistry. 2015-06, 7 (8): 979–988 [2022-03-09]. ISSN 1756-8919. doi:10.4155/fmc.15.48 (英語).
- ^ Christophe Pardin, Isabelle Roy, William D. Lubell, Jeffrey W. Keillor. Reversible and Competitive Cinnamoyl Triazole Inhibitors of Tissue Transglutaminase. Chemical Biology & Drug Design. 2008-09, 72 (3): 189–196 [2022-03-09]. doi:10.1111/j.1747-0285.2008.00696.x. (原始內容存檔於2022-03-09) (英語). (頁面存檔備份,存於互聯網檔案館)
- ^ Ruofeng Huang, Xiaohui Zhang, Jing Pan, Jiaqiang Li, Hang Shen, Xuege Ling, Yan Xiong. Benzylation of arenes with benzyl halides synergistically promoted by in situ generated superacid boron trifluoride monohydrate and tetrahaloboric acid. Tetrahedron. 2015-03, 71 (10): 1540–1546 [2022-03-09]. doi:10.1016/j.tet.2015.01.037. (原始內容存檔於2020-03-02) (英語). (頁面存檔備份,存於互聯網檔案館)