二噻英并二喹啉

维基百科,自由的百科全书
(重定向自C18H10N2S2
二噻英并二喹啉
IUPAC名
2,13-Dithia-10,21-diazapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4,6,8,10,15,17,19,21-decaene
别名 Thiochinathren
识别
CAS号 50634-27-0  checkY
PubChem 10870863
ChemSpider 9046144
SMILES
 
  • C1=CC=C2C(=C1)C3=C(C=N2)SC4=C(S3)C=NC5=CC=CC=C54
性质
化学式 C18H10N2S2
摩尔质量 318.42 g·mol−1
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

二噻英并二喹啉[1,4]二噻英并[2,3-c:5,6-c']二喹啉)是一种有机化合物,化学式为C18H10N2S2。它的异构体[1,4]二噻英并[2,3-c:6,5-c']二喹啉(异二噻英并二喹啉)是已知的[1],但它们的[1,2]二噻英英语Dithiin异构体是未知的。

它可以喹啉和2-氯-3-甲硫基喹啉、为原料反应得到。[2]它可以被硝酸-硫酸氧化为二噻英并二喹啉-S-氧化物。[3]

参考文献[编辑]

  1. ^ Andrzej Maślankiewicz, Krystian Pluta, Mirosław Wyszomirski, Adolf Gogoll, Maria J. Maślankiewicz. Complete assignment of the1H and13C NMR spectra of thioquinanthrene and isothioquinanthrene. Magnetic Resonance in Chemistry. 1998-01, 36 (1): 73–75 [2023-06-17]. ISSN 0749-1581. doi:10.1002/(SICI)1097-458X(199801)36:13.0.CO;2-Y (英语). 
  2. ^ Maslankiewicz, Andrzej. Sulfurization of azines. Part VII. Exhaustive sulfurization of quinoline. Polish Journal of Chemistry (1985), 59(5-6), 511-520.
  3. ^ Maslankiewicz, Maria J.; Glowiak, Tadeusz. Nitrothioquinanthrenes and their S-oxides. Heterocycles (2003), 60(6), 1387-1400.

拓展阅读[编辑]

  • Maslankiewicz, A.; Bebenek, E. Azinyl sulfides. Part LVII. The reaction of some dithiinodiquinolines with potassium methoxide as a source of 4-quinolinones with 3-sulfide function. Polish Journal of Chemistry, 1999. 73 (11): 1783-1789.