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CAS RN: 31366-25-3 | 产品编码: T0980
Tetrathiafulvalene
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| 产品编码 | T0980 |
| 纯度/分析方法 | >98.0%(GC) |
| 分子式/分子量 | C__6H__4S__4 = 204.34 |
| 外观与形状（20°C） | 固体 |
| 储存温度 | 室温 (15°C以下阴凉干燥处) |
| 储存在惰性气体下 | 存放于惰性气体之中 |
| 应避免的情况 | 光,空气 |
| 包装和容器 | 1G-Glass Bottle with Plastic Insert （查看图片） |
| CAS RN | 31366-25-3 |
| Reaxys-RN | 1282106 |
| PubChem物质ID | 87576791 |
| SDBS (AIST Spectral DB) | 13743 |
| Merck Index (14) | 9242 |
| MDL编号 | MFCD00005492 |
技术规格
| Appearance | Orange to Brown powder to crystal |
| Purity(GC) | min. 98.0 % |
| Melting point | 118.0 to 123.0 °C |
物性（参考值）
| 熔点 | 120 °C |
| 最大吸收波长 | 369 nm (CHCl__3) |
GHS
相关法规
运输信息
| HS编码* | 2934.99-000 |
应用
An Organic Electron Donor
Tetrathiafulvalene (TTF) was first synthesized by Wudl et al.1, 2) It works as an organic electron donor, and used for radical reactions by Murphy et al.3)
References
- 1)Bis-1,3-dithiolium chloride: an unusually stable organic radical cation
- 2)Electrical conductivity by the bis(1,3-dithiole)-bis(1,3-dithiolium) system
- 3)Tetrathiafulvalene as a catalyst for radical–polar crossover reactions
参考文献
