N,N-二苯基脲
N,N-二苯基脲 | |
---|---|
![]() | |
識別 | |
CAS號 | 603-54-3 ![]() |
性質 | |
化學式 | C13H12N2O |
摩爾質量 | 212.25 g·mol−1 |
熔點 | 189 °C(462 K)[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
N,N-二苯基脲也稱1,1-二苯基脲,它是一種有機化合物,化學式為C13H12N2O,是N,N '-二苯基脲的同分異構體。它可由二苯胺、氰酸鈉和三氟乙酸反應製得。[2]它和對甲苯磺酰氯在吡啶中反應,可以得到二苯基氨基氰[3];它和次氯酸鈉反應,得到1,1-二苯肼。[4]
參考文獻
- ^ "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. (原始內容存檔於2021-09-08) (英語).
- ^ 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 (英語).
- ^ 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 (英語).