4,7-二氨基-2,1,3-苯并噻二唑
| 中文名称 | 4,7-二氨基-2,1,3-苯并噻二唑 |
|---|---|
| 中文同义词 | 4,7-二氨基-2,1,3-苯并噻二唑;2,1,3-苯并噻二唑-4,7-二胺;苯并[C][1,2,5]噻二唑-4,7-二胺 |
| 英文名称 | 4,7-diamine-2,1,3-benzothiadiazole |
| 英文同义词 | 4,7-diamine-2,1,3-benzothiadiazole;Benzo[c][1,2,5]thiadiazole-4,7-diamine |
| CAS号 | 19951-39-4 |
| 分子式 | C6H6N4S |
| 分子量 | 166.2 |
| EINECS号 | |
| 相关类别 | 科研材料中间体 |
| Mol文件 | 19951-39-4.mol |
| 结构式 |  |
4,7-二氨基-2,1,3-苯并噻二唑 性质
| 熔点 | 128-130 °C |
|---|---|
| 沸点 | 387.4±22.0 °C(Predicted) |
| 密度 | 1.597±0.06 g/cm3(Predicted) |
| 酸度系数(pKa) | 2.32±0.10(Predicted) |
可作为单体用于合成COF材料：TH-COF-1
[2] A thiadiazole-functionalized covalent organic framework for efficient CO2 capture and separation. https://doi.org/10.1016/j.micromeso.2015.11.030
[3] 2Ch–2N square and hexagon interactions: a combined crystallographic data analysis and computational study. https://doi.org/10.1039/c9cp04562g
参考文献
[1] Preparation, Structure, and Amphoteric Redox Properties of p-Phenylenediamine-Type Dyes Fused with a Chalcogenadiazole Unit. https://doi.org/10.1021/jo010808h
[2] A thiadiazole-functionalized covalent organic framework for efficient CO2 capture and separation. https://doi.org/10.1016/j.micromeso.2015.11.030
[3] 2Ch–2N square and hexagon interactions: a combined crystallographic data analysis and computational study. https://doi.org/10.1039/c9cp04562g