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| 1158868-60-0

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1158868-60-0
化学式
C54H42I4O8
mdl
——
分子量
1326.54
InChiKey
JRHXAUYURXTDRL-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

物化性质

  • 熔点:
    247-249 °C
  • 密度:
    1.738±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    15.32
  • 重原子数:
    66.0
  • 可旋转键数:
    16.0
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    73.84
  • 氢给体数:
    0.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    盐酸 作用下, 以 甲醇氯仿 为溶剂, 反应 4.0h, 以99%的产率得到6-[4-[6-Hydroxy-5-(2-hydroxy-3-iodonaphthalen-1-yl)-7-iodonaphthalen-2-yl]phenyl]-1-(2-hydroxy-3-iodonaphthalen-1-yl)-3-iodonaphthalen-2-ol
    参考文献:
    名称:
    Self-supported BINOL–Zn catalysts for heterogeneous enantioselective epoxidation of (E)-α,β-unsaturated ketones
    摘要:
    A class of chiral self-supported catalysts prepared from bis-BINOL ligands and diethyl zinc were successfully applied in the hetereogeneous enantioselective epoxidation of a range of (E)-alpha,beta-unsaturated ketones, affording the corresponding epoxy ketones in high enantioselectivity. The self-supported catalysts were easily recovered from the reaction mixture and were reusable for several consecutive runs. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.02.151
  • 作为产物:
    描述:
    正丁基锂 作用下, 以 四氢呋喃乙醚正己烷 为溶剂, 以43%的产率得到
    参考文献:
    名称:
    Self-supported BINOL–Zn catalysts for heterogeneous enantioselective epoxidation of (E)-α,β-unsaturated ketones
    摘要:
    A class of chiral self-supported catalysts prepared from bis-BINOL ligands and diethyl zinc were successfully applied in the hetereogeneous enantioselective epoxidation of a range of (E)-alpha,beta-unsaturated ketones, affording the corresponding epoxy ketones in high enantioselectivity. The self-supported catalysts were easily recovered from the reaction mixture and were reusable for several consecutive runs. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.02.151
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