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2-[2-[4-[9-[4-[2-(2-Prop-2-enoxyethoxy)ethoxy]phenyl]-1,10-phenanthrolin-2-yl]phenoxy]ethoxy]ethanol | 1030607-06-7

中文名称
——
中文别名
——
英文名称
2-[2-[4-[9-[4-[2-(2-Prop-2-enoxyethoxy)ethoxy]phenyl]-1,10-phenanthrolin-2-yl]phenoxy]ethoxy]ethanol
英文别名
2-[2-[4-[9-[4-[2-(2-prop-2-enoxyethoxy)ethoxy]phenyl]-1,10-phenanthrolin-2-yl]phenoxy]ethoxy]ethanol
2-[2-[4-[9-[4-[2-(2-Prop-2-enoxyethoxy)ethoxy]phenyl]-1,10-phenanthrolin-2-yl]phenoxy]ethoxy]ethanol化学式
CAS
1030607-06-7
化学式
C35H36N2O6
mdl
——
分子量
580.681
InChiKey
QSOAVQVFEFLBKP-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):
    5.2
  • 重原子数:
    43
  • 可旋转键数:
    17
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    92.2
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    2-[2-[4-[9-[4-[2-(2-Prop-2-enoxyethoxy)ethoxy]phenyl]-1,10-phenanthrolin-2-yl]phenoxy]ethoxy]ethanol间苯二甲酰氯 在 Proton-Sponge 作用下, 以 二氯甲烷 为溶剂, 以66%的产率得到C78H74N4O14
    参考文献:
    名称:
    A double ring-closing olefin metathesis approach to [3]catenanes
    摘要:
    A [3]catenane with peripheral olefinic macrocycles was conveniently synthesized via a double ring-closing olefin metathesis. Highlights of this work include the synthesis of a 65-membered macrocycle featuring two phenanthroline ligands, a Cu(1)-templated synthesis of a [3]pseudorotaxane, and the key double ring-closing olefin metathesis to afford the desired [3]catenane in 71% yield. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.03.012
  • 作为产物:
    描述:
    3-溴丙烯 、 2-{2-[4-(9-{4-[2-(2-Hydroxy-ethoxy)-ethoxy]-phenyl}-[1,10]phenanthrolin-2-yl)-phenoxy]-ethoxy}-ethanol 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以67%的产率得到2-[2-[4-[9-[4-[2-(2-Prop-2-enoxyethoxy)ethoxy]phenyl]-1,10-phenanthrolin-2-yl]phenoxy]ethoxy]ethanol
    参考文献:
    名称:
    A double ring-closing olefin metathesis approach to [3]catenanes
    摘要:
    A [3]catenane with peripheral olefinic macrocycles was conveniently synthesized via a double ring-closing olefin metathesis. Highlights of this work include the synthesis of a 65-membered macrocycle featuring two phenanthroline ligands, a Cu(1)-templated synthesis of a [3]pseudorotaxane, and the key double ring-closing olefin metathesis to afford the desired [3]catenane in 71% yield. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.03.012
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文献信息

  • A double ring-closing olefin metathesis approach to [3]catenanes
    作者:Manav Gupta、Songsu Kang、Michael F. Mayer
    DOI:10.1016/j.tetlet.2008.03.012
    日期:2008.4
    A [3]catenane with peripheral olefinic macrocycles was conveniently synthesized via a double ring-closing olefin metathesis. Highlights of this work include the synthesis of a 65-membered macrocycle featuring two phenanthroline ligands, a Cu(1)-templated synthesis of a [3]pseudorotaxane, and the key double ring-closing olefin metathesis to afford the desired [3]catenane in 71% yield. (c) 2008 Elsevier Ltd. All rights reserved.
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