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2,2,3,3-tetrafluoro-2,3-dihydro-1H-cyclopenta[a]naphthalene | 922141-63-7

中文名称
——
中文别名
——
英文名称
2,2,3,3-tetrafluoro-2,3-dihydro-1H-cyclopenta[a]naphthalene
英文别名
2,2,3,3-Tetrafluoro-2,3-dihydro-1H-cyclopenta[a]naphthalene;2,2,3,3-tetrafluoro-1H-cyclopenta[a]naphthalene
2,2,3,3-tetrafluoro-2,3-dihydro-1H-cyclopenta[a]naphthalene化学式
CAS
922141-63-7
化学式
C13H8F4
mdl
——
分子量
240.2
InChiKey
UJANULSVOAONND-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:
    40-42 °C
  • 沸点:
    273.2±40.0 °C(Predicted)
  • 密度:
    1.36±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.3
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    sodium chlorodifluoroacetate1,1-二氟-2-(1-萘基)乙烯二乙二醇二甲醚 为溶剂, 反应 13.0h, 以79%的产率得到2,2,3,3-tetrafluoro-2,3-dihydro-1H-cyclopenta[a]naphthalene
    参考文献:
    名称:
    One-pot process to prepare 1,1,2,2-tetrafluoroindane from substituted 2,2-difluorostyrene and sodium chlorodifluoroacetate
    摘要:
    Reaction of 2,2-difluorostyrenes and sodium chlorodifluoroacetate in diglyme solution at 180 degrees C gave 1-aryl-2,2,3,3-tetrafluorocyclopropane as a primary product. After prolong reaction under the same condition, the 1, 1,2,2-tetrafluoroindanes can be isolated as the only product in good yields. All the tetrafluorocyclopropanes and tetrafluoroindanes were well characterized by spectroscopic analyses. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.10.041
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文献信息

  • One-pot process to prepare 1,1,2,2-tetrafluoroindane from substituted 2,2-difluorostyrene and sodium chlorodifluoroacetate
    作者:Chuan-Chen Lee、Shaw-Tao Lin、Shun-Ying Ke
    DOI:10.1016/j.tet.2006.10.041
    日期:2007.1
    Reaction of 2,2-difluorostyrenes and sodium chlorodifluoroacetate in diglyme solution at 180 degrees C gave 1-aryl-2,2,3,3-tetrafluorocyclopropane as a primary product. After prolong reaction under the same condition, the 1, 1,2,2-tetrafluoroindanes can be isolated as the only product in good yields. All the tetrafluorocyclopropanes and tetrafluoroindanes were well characterized by spectroscopic analyses. (c) 2006 Elsevier Ltd. All rights reserved.
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