N-(9H-carbazol-9-yl)-4-methylbenzeneamine | 71903-22-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: N-(9H-carbazol-9-yl)-4-methylbenzeneamine
• 英文别名: N-(Carbazol-9-yl)-4-toluidin；carbazol-9-yl-p-tolyl-amine；N-(4-methylphenyl)carbazol-9-amine
• CAS: 71903-22-5
• 化学式: C₁₉H₁₆N₂
• 分子量: 272.349
• InChiKey: XLZXAXNVYIKDJL-UHFFFAOYSA-N

物化性质

• 沸点：
  457.9±38.0 °C(Predicted)
• 密度：
  1.13±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  17
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  2-氨基-2’-碘联苯 在 三正丁基氢锡 、 溶剂黄146 作用下， 以 苯 为溶剂， 反应 25.0h， 生成 N-(9H-carbazol-9-yl)-4-methylbenzeneamine
  参考文献：
  名称：

  Reaction of azoarenes with tributyltin hydride

  摘要：

  Tributyltin hydride when reacted with a series of substituted azoarenes afforded hydrazo compounds with high chemoselectivity and good to high yields. With ortho-substituted azoarenes, mixtures of hydrazo derivatives and N-heterocycles or cyclic products only were obtained. The kinetic law of the process was determined in the presence and in the absence of AIBN; with the radical initiator the reaction proceeds via a radical chain mechanism, whereas without AIBN the presence of stannyl free radicals could be discarded. The mechanism of the noninitiated reaction is discussed. EPR characterization of spin adducts obtained by reacting group IVB organometallic radicals with azo compounds is reported.

  DOI：

  10.1021/jo00028a038

文献信息

• 신규한 유기 화합물 및 이를 포함하는 유기 발광 소자
  申请人：SFC CO., LTD. 에스에프씨 주식회사(120060087061) Corp. No ▼ 135511-0105889BRN ▼134-81-54429

  公开号：KR20180024306A

  公开（公告）日：2018-03-08

  본 발명은 [화학식 A] 내지 [화학식 D] 중 어느 하나로 표시되는 유기 화합물 및 이를 포함하는 유기발광소자에 관한 것으로서, 상기 [화학식 A] 내지 [화학식 D]에서, X, R1 내지 R12, L1, L2, Ar1 내지 Ar3, n 및 m은 발명의 상세한 설명에 기재된 바와 같다. [화학식 A] [화학식 B] [화학식 C] [화학식 D]

  This is the Chinese translation of the text you provided: 本发明涉及一种有机化合物和包含该有机化合物的有机发光器件，所述有机化合物表示为[化学式A]至[化学式D]中的任何一个，在所述[化学式A]至[化学式D]中，X，R1至R12，L1，L2，Ar1至Ar3，n和m如本发明详细描述中所述。 [化学式A] [化学式B] [化学式C] [化学式D]