N,N-二苯基脲

化合物

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]

N,N-二苯基脲
识别
CAS号 603-54-3  checkY
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。

参考文献

编辑
  1. ^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2021-09-08].
  2. ^ 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). 
  3. ^ 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). 
  4. ^ 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).