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3-fluoro-2-hydroxy-5-perfluorooctylbenzaldehyde | 1254926-98-1

中文名称
——
中文别名
——
英文名称
3-fluoro-2-hydroxy-5-perfluorooctylbenzaldehyde
英文别名
3-Fluoro-5-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl)-2-hydroxybenzaldehyde
3-fluoro-2-hydroxy-5-perfluorooctylbenzaldehyde化学式
CAS
1254926-98-1
化学式
C15H4F18O2
mdl
——
分子量
558.167
InChiKey
JCXRYOJNHNGEKW-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:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    20

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and RCM Reactions Using a Recyclable Grubbs−Hoveyda Metathesis Catalyst Activated by a Light Fluorous Tag
    摘要:
    A recyclable Grubbs-Hoveyda second-generation catalyst activated by a light fluorous tag was prepared The modified light fluorous catalyst exhibited higher catalytic activity than the parent or the previously reported light fluorous variant for RCM reactions and could be routinely recovered The light fluorous tag incorporated in the catalyst served as both an activator as well as a handle for separation and recovery with fluorous solid-phase extraction
    DOI:
    10.1021/jo101140w
  • 作为产物:
    描述:
    全氟辛基碘烷3-氟-2-羟基苯甲醛偶氮二甲氧基异庚腈caesium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 20.0h, 以12%的产率得到3-fluoro-2-hydroxy-5-perfluorooctylbenzaldehyde
    参考文献:
    名称:
    Synthesis and RCM Reactions Using a Recyclable Grubbs−Hoveyda Metathesis Catalyst Activated by a Light Fluorous Tag
    摘要:
    A recyclable Grubbs-Hoveyda second-generation catalyst activated by a light fluorous tag was prepared The modified light fluorous catalyst exhibited higher catalytic activity than the parent or the previously reported light fluorous variant for RCM reactions and could be routinely recovered The light fluorous tag incorporated in the catalyst served as both an activator as well as a handle for separation and recovery with fluorous solid-phase extraction
    DOI:
    10.1021/jo101140w
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