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蒽嵌蒽醌

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蒽嵌蒽醌
别名 Anthanthrone orange
识别
CAS号 641-13-4  checkY
PubChem 94183
ChemSpider 84997
SMILES
 
  • C1=CC2=C3C(=C1)C(=O)C4=C5C3=C(C=C2)C(=O)C6=CC=CC(=C65)C=C4
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-萘内酰亚胺英语naphthostyril(或1,1'-联萘-8,8'-二甲酸[1])为原料制得。[2][3]蒽嵌蒽重铬酸钠氧化,也能得到蒽嵌蒽醌。[4]

参考文献

  1. ^ 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). 
  2. ^ Hunger, K.; Herbst, W., Pigments, Organic, Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, 2005, doi:10.1002/14356007.a20_371 
  3. ^ 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可免费查阅. 
  4. ^ 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).