N,N-二苯基脲
外观
N,N-二苯基脲 | |
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识别 | |
CAS号 | 603-54-3 ![]() |
性质 | |
化学式 | C13H12N2O |
摩尔质量 | 212.25 g·mol−1 |
熔点 | 189 °C(462 K)[1] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
N,N-二苯基脲也称1,1-二苯基脲,它是一种有机化合物,化学式为C13H12N2O,是N,N '-二苯基脲的同分异构体。它可由二苯胺、氰酸钠和三氟乙酸反应制得。[2]它和对甲苯磺酰氯在吡啶中反应,可以得到二苯基氨基氰[3];它和次氯酸钠反应,得到1,1-二苯肼。[4]
参考文献
[编辑]- ^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2021-09-08].
- ^ Yasuoki Murakami, Yuusaku Yokoyama, Chiyoko Sasakura, Makiko Tamagawa. An efficient synthesis of 1,1-disubstituted hydrazines.. Chemical and Pharmaceutical Bulletin. 1983, 31 (2): 423–428 [2021-09-08]. ISSN 0009-2363. doi:10.1248/cpb.31.423. (原始内容存档于2021-09-08) (英语).
- ^ Frederick Kurzer. 639. Cyanamides. Part III. The formation of substituted triazines from o-halogenophenylureas and arylsulphonyl chlorides. Journal of the Chemical Society (Resumed). 1949: 3033 [2021-09-08]. ISSN 0368-1769. doi:10.1039/jr9490003033 (英语).
- ^ Yasuoki Murakami, Yuusaku Yokoyama. An Efficient Method for Synthesis of 1,1-Diarylhydrazines as an Intermediate for Indole Synthesis. HETEROCYCLES. 1979, 12 (12): 1571 [2021-09-08]. ISSN 0385-5414. doi:10.3987/R-1979-12-1571 (英语).