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2-[3-(6-Chloro-pyridin-3-yl)-phenyl]-9-(4-methoxy-phenyl)-[1,10]phenanthroline | 350489-41-7

中文名称
——
中文别名
——
英文名称
2-[3-(6-Chloro-pyridin-3-yl)-phenyl]-9-(4-methoxy-phenyl)-[1,10]phenanthroline
英文别名
2-[3-(6-Chloropyridin-3-yl)phenyl]-9-(4-methoxyphenyl)-1,10-phenanthroline;2-[3-(6-chloropyridin-3-yl)phenyl]-9-(4-methoxyphenyl)-1,10-phenanthroline
2-[3-(6-Chloro-pyridin-3-yl)-phenyl]-9-(4-methoxy-phenyl)-[1,10]phenanthroline化学式
CAS
350489-41-7
化学式
C30H20ClN3O
mdl
——
分子量
473.961
InChiKey
AMTZPYVYJJNBPK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    7.3
  • 重原子数:
    35
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.03
  • 拓扑面积:
    47.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    6'-Bromo-5-(4-methoxy-phenyl)-[2,2']bipyridinyl2-[3-(6-Chloro-pyridin-3-yl)-phenyl]-9-(4-methoxy-phenyl)-[1,10]phenanthroline 在 NaSnMe3四(三苯基膦)钯 作用下, 以 乙二醇二甲醚甲苯 为溶剂, 反应 30.0h, 生成 5-(4-Methoxy-phenyl)-5''-{3-[9-(4-methoxy-phenyl)-[1,10]phenanthrolin-2-yl]-phenyl}-[2,2';6',2'']terpyridine
    参考文献:
    名称:
    Synthesis of multifunctional ligands: a 2,9-diaryl-1,10-phenanthroline/2,2′:6′,2″-terpyridine conjugate
    摘要:
    The synthesis of a ligand including a 1,10-phenanthroline and a 2,2':6',2"-terpyridine separated by a 1,3-phenylene spacer is presented. The different aromatic carbon-carbon bonds have been generated by reactions with organolithium compounds, and by Stille and Suzuki couplings. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)00279-9
  • 作为产物:
    描述:
    5-溴-2-氯吡啶四(三苯基膦)钯正丁基锂 、 sodium carbonate 作用下, 以 乙醚甲苯 为溶剂, 反应 32.5h, 生成 2-[3-(6-Chloro-pyridin-3-yl)-phenyl]-9-(4-methoxy-phenyl)-[1,10]phenanthroline
    参考文献:
    名称:
    Synthesis of multifunctional ligands: a 2,9-diaryl-1,10-phenanthroline/2,2′:6′,2″-terpyridine conjugate
    摘要:
    The synthesis of a ligand including a 1,10-phenanthroline and a 2,2':6',2"-terpyridine separated by a 1,3-phenylene spacer is presented. The different aromatic carbon-carbon bonds have been generated by reactions with organolithium compounds, and by Stille and Suzuki couplings. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)00279-9
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文献信息

  • Synthesis of multifunctional ligands: a 2,9-diaryl-1,10-phenanthroline/2,2′:6′,2″-terpyridine conjugate
    作者:Nicolas Belfrekh、Christiane Dietrich-Buchecker、Jean-Pierre Sauvage
    DOI:10.1016/s0040-4039(01)00279-9
    日期:2001.4
    The synthesis of a ligand including a 1,10-phenanthroline and a 2,2':6',2"-terpyridine separated by a 1,3-phenylene spacer is presented. The different aromatic carbon-carbon bonds have been generated by reactions with organolithium compounds, and by Stille and Suzuki couplings. (C) 2001 Elsevier Science Ltd. All rights reserved.
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