蒽嵌蒽醌
| 蒽嵌蒽醌 | |
|---|---|
| |
| 别名 | Anthanthrone orange |
| 识别 | |
| CAS号 | 641-13-4 
|
| PubChem | 94183 |
| ChemSpider | 84997 |
| SMILES |
|
| 性质 | |
| 化学式 | C22H10O2 |
| 摩尔质量 | 306.31 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
蒽嵌蒽醌是一种有机化合物，化学式为C22H10O2，可用作颜料红168的前体。它可由1,8-萘内酰亚胺（或1,1'-联萘-8,8'-二甲酸[1]）为原料制得。[2][3]蒽嵌蒽经重铬酸钠氧化，也能得到蒽嵌蒽醌。[4]
参考文献
- ^ D Thetford, A.P Chorlton. Investigation of vat dyes as potential high performance pigments. Dyes and Pigments. 2004-04, 61 (1): 49–62 [2021-01-04]. doi:10.1016/j.dyepig.2003.09.002. （原始内容存档于2018-06-26） （英语）.
- ^ Hunger, K.; Herbst, W., Pigments, Organic, Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, 2005, doi:10.1002/14356007.a20_371
- ^ Edwards, I. A. S.; Stadler, H. P. The crystal structure of anthanthrone. Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 1971, 27 (5): 946–952. doi:10.1107/S0567740871003303
.
- ^ Karl L. Platt, Christian Degenhardt, Stefanie Grupe, Heinz Frank, Albrecht Seidel. Microsomal Activation of Dibenzo[ def , mno ]chrysene (Anthanthrene), a Hexacyclic Aromatic Hydrocarbon without a Bay-Region, to Mutagenic Metabolites. Chemical Research in Toxicology. 2002-03, 15 (3): 332–342 [2021-01-04]. ISSN 0893-228X. doi:10.1021/tx010131t （英语）.
