1,5-二溴蒽
1,5-二溴蒽 | |
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識別 | |
CAS號 | 3278-82-8 |
SMILES |
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性質 | |
化學式 | C14H8Br2 |
摩爾質量 | 336.02 g·mol−1 |
外觀 | 黃色固體[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
1,5-二溴蒽是一種有機化合物,化學式為C14H8Br2,它可由1,5-二氨基蒽醌和溴化銅的乙腈溶液和亞硝酸叔丁酯反應,經硫酸酸化、硼氫化鈉還原得到。[1]它和三甲基矽基乙炔在催化下反應,可以得到1,5-二(三甲基矽基乙炔基)蒽。[2]
參考文獻
- ^ 1.0 1.1 Feofanov, Mikhail; Akhmetov, Vladimir; Sharapa, Dmitry I.; Amsharov, Konstantin. Modular Approach to the Synthesis of Two-Dimensional Angular Fused Acenes. Organic Letters. 2020-03-06, 22 (5): 1698–1702. ISSN 1523-7060. doi:10.1021/acs.orglett.9b04382.
- ^ Iseki, Shuta; Nonomura, Kohei; Kishida, Sakura; Ogata, Daiji; Yuasa, Junpei. Zinc-Ion-Stabilized Charge-Transfer Interactions Drive Self-Complementary or Complementary Molecular Recognition. Journal of the American Chemical Society. 2020-09-16, 142 (37): 15842–15851. ISSN 0002-7863. doi:10.1021/jacs.0c05940.