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1α-Hydroxy-1-epiprobotrydial | 158675-35-5

中文名称
——
中文别名
——
英文名称
1α-Hydroxy-1-epiprobotrydial
英文别名
——
1α-Hydroxy-1-epiprobotrydial化学式
CAS
158675-35-5
化学式
C15H24O
mdl
——
分子量
220.355
InChiKey
CJLPUCOCOGMEFJ-UXOAXIEHSA-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):
    3.53
  • 重原子数:
    16.0
  • 可旋转键数:
    0.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.87
  • 拓扑面积:
    20.23
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

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
  • 下游产品
    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:
    1α-Hydroxy-1-epiprobotrydialWilkinson's catalyst 作用下, 以 乙醇 为溶剂, 反应 80.0h, 以84%的产率得到(-)-presilphiperfolan-1-ol
    参考文献:
    名称:
    Synthesis and antifungal activity of analogues of naturally occurring botrydial precursors
    摘要:
    Analog compounds of the proposed intermediates of the biogenetic pathway to botrydial have been synthesized. These compounds were tested for their potential antifungal activity against the phytopathogen Botrytis cinerea. Our results showed a fungistatic effect of some compounds on mycelium growth. The most significant effect was exerted by 2-alpha-hydroxy-2,3-dihydro-1-epiprobotrydial, which inhibited growth of B. cinerea. Some aspects of structure-activity relationships are discussed.
    DOI:
    10.1007/bf02036197
  • 作为产物:
    描述:
    1-Epiprobotrydial叔丁基过氧化氢 、 selenium(IV) oxide 作用下, 以 二氯甲烷 为溶剂, 以16%的产率得到1α-Hydroxy-1-epiprobotrydial
    参考文献:
    名称:
    Synthesis and antifungal activity of analogues of naturally occurring botrydial precursors
    摘要:
    Analog compounds of the proposed intermediates of the biogenetic pathway to botrydial have been synthesized. These compounds were tested for their potential antifungal activity against the phytopathogen Botrytis cinerea. Our results showed a fungistatic effect of some compounds on mycelium growth. The most significant effect was exerted by 2-alpha-hydroxy-2,3-dihydro-1-epiprobotrydial, which inhibited growth of B. cinerea. Some aspects of structure-activity relationships are discussed.
    DOI:
    10.1007/bf02036197
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