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3-chlorocyclo[7.1.0.02,4]dec-2-ene | 245517-52-6

中文名称
——
中文别名
——
英文名称
3-chlorocyclo[7.1.0.02,4]dec-2-ene
英文别名
3-Chlorotricyclo[7,1,0,0 2,4]dec-2-ene;10-chlorotricyclo[7.1.0.02,4]dec-1(10)-ene
3-chlorocyclo[7.1.0.0<sup>2,4</sup>]dec-2-ene化学式
CAS
245517-52-6
化学式
C10H13Cl
mdl
——
分子量
168.666
InChiKey
YQEDECMDPKEXTF-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):
    3.2
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    3-chlorocyclo[7.1.0.02,4]dec-2-ene 反应 1.0h, 生成 3-chlorobicyclo[7.1.0]deca-1,4-diene
    参考文献:
    名称:
    Dehydrohalogenation of adducts of dichlorocarbene with cyclooctene and its peripherally cyclopropanated analogs
    摘要:
    Dehydrohalogenation of three isomeric adducts of dichlorocarbene with bicyclo[6.1.0]non-1-, -2-, and -4-enes under the action of potassium tert-butoxide in DMSO was studied. In the course of dehydrohalogenation of the substrates under study, different isomerization processes, which were accompanied by repeated migrations of multiple bonds that formed, occurred depending on the structure of dichlorides, while no skeletal rearrangements were observed.
    DOI:
    10.1007/bf02494639
  • 作为产物:
    参考文献:
    名称:
    Dehydrohalogenation of adducts of dichlorocarbene with cyclooctene and its peripherally cyclopropanated analogs
    摘要:
    Dehydrohalogenation of three isomeric adducts of dichlorocarbene with bicyclo[6.1.0]non-1-, -2-, and -4-enes under the action of potassium tert-butoxide in DMSO was studied. In the course of dehydrohalogenation of the substrates under study, different isomerization processes, which were accompanied by repeated migrations of multiple bonds that formed, occurred depending on the structure of dichlorides, while no skeletal rearrangements were observed.
    DOI:
    10.1007/bf02494639
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