Dinitrooxythallanyl nitrate

• 分子结构分类: 无机化合物 - 混合金属/非金属化合物 - 后过渡金属氧阴离子化合物
• 英文名称: Dinitrooxythallanyl nitrate
• 化学式: N3O9Tl
• 分子量: 390.4
• InChiKey: KLBIUKJOZFWCLW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.1
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  189
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  5-(pyridin-2-yl)-2,4-dihydro-3H-pyrazol-3-one 、 Dinitrooxythallanyl nitrate 以80%的产率得到
  参考文献：
  名称：

  COSSY J.; PETE J.-P., BULL. SOC. CHIM. FRANCE, 1979, PART 2, NO 9-10, 559-567

  摘要：

  DOI：
• 作为产物：
  描述：

  thallium(I) nitrate 、 硝酸 生成 Dinitrooxythallanyl nitrate
  参考文献：
  名称：

  AIDZAVA, TAKAO

  摘要：

  DOI：

文献信息

• Anti-inflammatory and analgesic benzothiophene and benzafuran
  申请人：Beecham Group p.l.c.

  公开号：US04548948A1

  公开（公告）日：1985-10-22

  Compounds of formula (I): ##STR1## wherein: Ar is phenyl optionally substituted in the o-, m- or p-position by C.sub.1-4 alkyl, C.sub.1-4 alkoxy, trifluoromethyl, bromo, chloro or fluoro, pyrryl optionally N-substituted by C.sub.1-4 alkyl, 2-furyl or 2-thienyl either optionally substituted in the 3-, 4- or 5-position by methyl, chloro or bromo, or 3-furyl or 3-thienyl; X is oxygen, sulphur, sulphoxide or sulphone, Y is methylene, R.sub.1 and R.sub.3 are hydrogen or C.sub.1-4 alkyl, and R.sub.2 is hydrogen, C.sub.1-4 alkyl, fluoro, chloro or bromo, or X is methylene, Y is oxygen, R.sub.1 and R.sub.3 are both hydrogen, and R.sub.2 is hydrogen, fluoro, chloro or bromo; and R.sub.4 is hydrogen or C.sub.1-4 alkyl, or a salt thereof, have analgesic and/or anti-inflammatory activity.

  式(I)的化合物：## STR1 ## 其中：Ar是苯基，可以在o-、m-或p-位置上被C.sub.1-4烷基，C.sub.1-4烷氧基，三氟甲基，溴，氯或氟取代，也可以是吡咯基，可选择由C.sub.1-4烷基取代，2-呋喃基或2-噻吩基，也可以在3-、4-或5-位置上被甲基，氯或溴取代，或3-呋喃基或3-噻吩基；X是氧，硫，亚砜或砜，Y是亚甲基，R.sub.1和R.sub.3是氢或C.sub.1-4烷基，R.sub.2是氢，C.sub.1-4烷基，氟，氯或溴，或X是亚甲基，Y是氧，R.sub.1和R.sub.3都是氢，R.sub.2是氢，氟，氯或溴；R.sub.4是氢或C.sub.1-4烷基，或其盐，具有镇痛和/或抗炎活性。
• 3-Amino chroman and 2-amino tetralin derivatives
  申请人：Hatzenbuhler Theriault Nicole

  公开号：US20050032873A1

  公开（公告）日：2005-02-10

  3-Amino chroman and 2-amino tetralin derivatives and compositions containing such compounds are disclosed. Methods of using the 3-amino chroman and 2-amino tetralin compounds and compositions containing such compounds in the treatment of serotonin disorders, such as depression and anxiety, are also disclosed.

  本文披露了3-氨基色满和2-氨基四氢萘衍生物及含有这些化合物的组合物。还披露了使用3-氨基色满和2-氨基四氢萘化合物及含有这些化合物的组合物治疗血清素失调症，如抑郁和焦虑的方法。
• LIQUID CRYSTAL COMPOUNDS AND METHOD FOR PREPARING THE SAME
  申请人：Choi Kyung-Hee

  公开号：US20110237849A1

  公开（公告）日：2011-09-29

  The present invention relates to a liquid crystal compound for liquid crystal display. More particularly, the present invention provides a vinylcyclohexylbenzene, its derivatives and the preparation method thereof where the present invention produces only trans-isomer by using Heck coupling reaction instead of Wittig reaction in the introduction to ethenyl group in the central backbone in the preparation process of intermediate. The liquid crystal compound can make the liquid crystal composition have a wide mesophase range and low viscosity.

  本发明涉及一种用于液晶显示的液晶化合物。更具体地，本发明提供了一种乙烯基环己基苯及其衍生物以及其制备方法，其中本发明在中间体的制备过程中，使用Heck偶联反应而非Wittig反应，在中心骨架中引入乙烯基，从而仅产生顺式异构体。该液晶化合物可以使液晶组成物具有宽广的向列相范围和低粘度。
• Liquid crystal compounds and method for preparing the same
  申请人：Choi Kyung-Hee

  公开号：US08512598B2

  公开（公告）日：2013-08-20

  The present invention relates to a liquid crystal compound for liquid crystal display. More particularly, the present invention provides a vinylcyclohexylbenzene, its derivatives and the preparation method thereof where the present invention produces only trans-isomer by using Heck coupling reaction instead of Wittig reaction in the introduction to ethenyl group in the central backbone in the preparation process of intermediate. The liquid crystal compound can make the liquid crystal composition have a wide mesophase range and low viscosity.

  本发明涉及用于液晶显示器的液晶化合物。更具体地说，本发明提供了一种乙烯基环己基苯，其衍生物及其制备方法，其中本发明在中间体制备过程中，在引入中央骨架中的乙烯基团时，使用Heck偶联反应而不是Wittig反应，仅产生顺式异构体。此液晶化合物可使液晶组成物具有广泛的介相范围和低粘度。
• TAYLOR E. C.; TURCHI I. J.; MCKILLOP A., HETEROCYCLES, SPEC. ISSUE, 1978, NO 11, 481-487
  作者：TAYLOR E. C.、 TURCHI I. J.、 MCKILLOP A.

  DOI：——

  日期：——