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| 183118-58-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
183118-58-3
化学式
C11H16O2Si
mdl
——
分子量
208.332
InChiKey
LQNOJYWSILZOCH-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):
    2.28
  • 重原子数:
    14.0
  • 可旋转键数:
    4.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    22.37
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    四氢呋喃乙腈 为溶剂, 85.0 ℃ 、999.99 MPa 条件下, 反应 45.0h, 以47%的产率得到endo-3,12-dioxatetracyclo[7.2.1.01,705,7]dodec-10-ene
    参考文献:
    名称:
    Intramolecular Diels-Alder reactions of furans with a merely strain-activated tetrasubstituted alkene: Bicyclopropylidene
    摘要:
    Bicyclopropylidene derivatives 1, 6, 8 with furan moieties attached on tethers of various length and nature all undergo clean intramolecular Diels-Alder reactions with complete endo-diastereoselectivities when heated to 70 - 130 degrees C, under 10 kbar pressure. The reaction rates are at]east as high or higher than those of analogously tethered methylenecyclopropane-furan derivatives 15, 17, 20, in spite of the fact that the reactive double bond in bicyclopropylidene is tetrasubstituted and not activated by any electron withdrawing group. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/0040-4020(96)00720-x
  • 作为产物:
    描述:
    (2-亚甲基环丙基)甲醇Chlor-2-furanyl-dimethylsilan三乙胺 作用下, 以 乙醚 为溶剂, 以99%的产率得到
    参考文献:
    名称:
    Intramolecular Diels-Alder reactions of furans with a merely strain-activated tetrasubstituted alkene: Bicyclopropylidene
    摘要:
    Bicyclopropylidene derivatives 1, 6, 8 with furan moieties attached on tethers of various length and nature all undergo clean intramolecular Diels-Alder reactions with complete endo-diastereoselectivities when heated to 70 - 130 degrees C, under 10 kbar pressure. The reaction rates are at]east as high or higher than those of analogously tethered methylenecyclopropane-furan derivatives 15, 17, 20, in spite of the fact that the reactive double bond in bicyclopropylidene is tetrasubstituted and not activated by any electron withdrawing group. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/0040-4020(96)00720-x
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