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(Z)-13-(oxan-2-yloxy)tridec-4-en-2-yn-1-ol | 1048005-48-6

中文名称
——
中文别名
——
英文名称
(Z)-13-(oxan-2-yloxy)tridec-4-en-2-yn-1-ol
英文别名
——
(Z)-13-(oxan-2-yloxy)tridec-4-en-2-yn-1-ol化学式
CAS
1048005-48-6
化学式
C18H30O3
mdl
——
分子量
294.434
InChiKey
JYMZGGSVJYKYIH-XQRVVYSFSA-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):
    4.3
  • 重原子数:
    21
  • 可旋转键数:
    10
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (Z)-13-(oxan-2-yloxy)tridec-4-en-2-yn-1-olmanganese(IV) oxide 作用下, 以52%的产率得到(Z)-13-(oxan-2-yloxy)tridec-4-en-2-ynal
    参考文献:
    名称:
    (9Z)-9,13-Tetradecadien-11-ynal, the sex pheromone of the avocado seed moth, Stenoma catenifer
    摘要:
    The highly unsaturated aldehyde (9Z)-9,13-tetradecadien-11-ynal and the corresponding alcohol were identified as possible sex pheromone components of the avocado seed moth, Stenoma catenifer. The aldehyde as a single component attracted more male moths than caged virgin female moths, and addition of the analogous alcohol and/or acetate decreased attraction. A stereospecific synthesis of the pheromone is described. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.06.019
  • 作为产物:
    描述:
    (Z)-10-Iodo-1-(2-tetrahydropyranyloxy)-9-decene2-丙炔-1-醇四氢吡咯 、 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 作用下, 以86%的产率得到(Z)-13-(oxan-2-yloxy)tridec-4-en-2-yn-1-ol
    参考文献:
    名称:
    (9Z)-9,13-Tetradecadien-11-ynal, the sex pheromone of the avocado seed moth, Stenoma catenifer
    摘要:
    The highly unsaturated aldehyde (9Z)-9,13-tetradecadien-11-ynal and the corresponding alcohol were identified as possible sex pheromone components of the avocado seed moth, Stenoma catenifer. The aldehyde as a single component attracted more male moths than caged virgin female moths, and addition of the analogous alcohol and/or acetate decreased attraction. A stereospecific synthesis of the pheromone is described. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.06.019
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