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ethyl 3-ethylhex-2-enoate | 1150667-94-9

中文名称
——
中文别名
——
英文名称
ethyl 3-ethylhex-2-enoate
英文别名
Ethyl 3-ethylhex-2-enoate
ethyl 3-ethylhex-2-enoate化学式
CAS
1150667-94-9
化学式
C10H18O2
mdl
——
分子量
170.252
InChiKey
AMDBYGYJCYMGJR-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):
    3.3
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    ethyl 3-ethylhex-2-enoate 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 反应 4.0h, 以85%的产率得到3-ethylhex-2-en-1-ol
    参考文献:
    名称:
    Synthesis and biological activity of permethrinic acid analogs containing various substituents in position 2 of the cyclopropane ring
    摘要:
    A number of permethrinic acid ethyl ester derivatives having various substituents [Et, Pr, Ph, Ph(CH2)n (n = 1, 2), etc.] in position 2 of the cyclopropane ring were synthesized, and their insecticidal acivity against typhoid flies., rice weevils, and bean aphides, as well as juvenoid activity on flour beetle chrysalises, was studied. The newly synthesized Compounds turned out to exhibit weak insecticidal activity against standard insects but pronounced juvenile hormone activity, which differentiates them from permethrinic acid esters.
    DOI:
    10.1134/s107042800808006x
  • 作为产物:
    描述:
    磷酰基乙酸三乙酯3-己酮potassium tert-butylate 作用下, 以 为溶剂, 反应 12.0h, 以76%的产率得到ethyl 3-ethylhex-2-enoate
    参考文献:
    名称:
    Synthesis and biological activity of permethrinic acid analogs containing various substituents in position 2 of the cyclopropane ring
    摘要:
    A number of permethrinic acid ethyl ester derivatives having various substituents [Et, Pr, Ph, Ph(CH2)n (n = 1, 2), etc.] in position 2 of the cyclopropane ring were synthesized, and their insecticidal acivity against typhoid flies., rice weevils, and bean aphides, as well as juvenoid activity on flour beetle chrysalises, was studied. The newly synthesized Compounds turned out to exhibit weak insecticidal activity against standard insects but pronounced juvenile hormone activity, which differentiates them from permethrinic acid esters.
    DOI:
    10.1134/s107042800808006x
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文献信息

  • Synthesis and biological activity of permethrinic acid analogs containing various substituents in position 2 of the cyclopropane ring
    作者:N. S. Mirzabekova、N. E. Kuz’mina、O. I. Lukashov、N. A. Sokolova、S. N. Golosov、P. V. Kazakov、T. G. Perlova、V. V. Potapova、V. A. Kheinman、G. B. Ivanova
    DOI:10.1134/s107042800808006x
    日期:2008.8
    A number of permethrinic acid ethyl ester derivatives having various substituents [Et, Pr, Ph, Ph(CH2)n (n = 1, 2), etc.] in position 2 of the cyclopropane ring were synthesized, and their insecticidal acivity against typhoid flies., rice weevils, and bean aphides, as well as juvenoid activity on flour beetle chrysalises, was studied. The newly synthesized Compounds turned out to exhibit weak insecticidal activity against standard insects but pronounced juvenile hormone activity, which differentiates them from permethrinic acid esters.
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