环戊烯并［cd］芘
| 环戊烯并［cd］芘 | |
|---|---|
| |
| IUPAC名 Cyclopenta[cd]pyrene | |
| 别名 | Acepyrene; pentacyclo[12.3.1.04,17.07,16.010,15]octadeca-1(18),2,4(17),5,7(16),8,10(15),11,13-nonaene |
| 识别 | |
| CAS号 | 27208-37-3 
|
| PubChem | 33743 |
| ChemSpider | 31107 |
| SMILES |
|
| ChEBI | 82279 |
| KEGG | C19173 |
| 性质 | |
| 化学式 | C18H10 |
| 摩尔质量 | 226.27 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
环戊烯并[cd]芘是一种有机化合物，化学式为C18H10。它可以1,8-二乙炔基蒽为原料，经多步反应制得。[1]它催化加氢可以得到3,4-二氢环戊烯并[cd]芘。[2]
参考文献
[编辑]- ^ Martin Sarobe; Leonardus W. Jenneskens. High-Temperature Behavior of 1,8-Diethynylanthracene. Benz[mno]aceanthrylene, a Transient Intermediate for Cyclopenta[cd]pyrene. J. Org. Chem. 1997, 62, 23, 8247–8250. doi:10.1021/jo970654z.
- ^ Sangaiah, R.; Gold, A.; Ball, L. M. Synthesis and mutagenicity of cyclopenta[cd]pyrene and its monomethyl derivatives. Polycyclic Aromatic Compounds, 1993. 3: 167-174. ISSN 1040-6638.