4-二甲氨基苯硫酚
4-二甲氨基苯硫酚是一種硫酚類有機化合物，化學式為C8H11NS。它可由硫氰酸(4-二甲氨基苯酯)的還原反應製得。[2][3]它可以被過氧化氫氧化，生成二(4-二甲氨基苯基)二硫化物。[4]
| 4-二甲氨基苯硫酚 | |
|---|---|
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| |
| 識別 | |
| CAS號 | 4946-22-9 
|
| 性質 | |
| 化學式 | C8H11NS |
| 摩爾質量 | 153.24 g·mol−1 |
| 外觀 | 淺黃色固體[1] |
| 熔點 | 32 °C[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
參考文獻
編輯- ^ 1.0 1.1 Christopher S. Argyle and G. Malcolm Dyson. The constitution and reactions of thiocarbonyl tetrachloride. Part IV. Reaction with secondary and tertiary amines. Journal of the Chemical Society (Resumed). 1937, 1629-1634. doi:10.1039/JR9370001629.
- ^ Gal Segalovich-Gerendash, Illya Rozenberg, Nebal Alassad, Noy B. Nechmad, Israel Goldberg, Sebastian Kozuch, and N. Gabriel Lemcoff. mposing Latency in Ruthenium Sulfoxide-Chelated Benzylidenes: Expanding Opportunities for Thermal and Photoactivation in Olefin Metathesis. ACS Catal. 2020, 10, 8, 4827–4834. doi:10.1021/acscatal.0c00676
- ^ David E. Bergbreiter, Jonathon D. Frels, Jeffrey Rawson, Jun Li, Joseph H. Reibenspies. Synthesis and characterization of electronically varied XCX palladacycles with functional arene groups. Inorg. Chim. Acta. 2006. 359 (6). 1912-1922. doi:10.1016/j.ica.2005.09.030.
- ^ Glen G. Briand, Reagan J. Davidson, and Andreas Decken. Substituent Effects on Indium−Phosphorus Bonding in (4-RC6H4S)3In·PR'3 Adducts (R = H, Me, F; R' = Et, Cy, Ph): A Spectroscopic, Structural, and Thermal Decomposition Study. Inorg. Chem. 2005, 44, 26, 9914–9920. doi:10.1021/ic051138r.