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3-Allyl-2-methyl-cyclopent-2-enol | 645421-44-9

中文名称
——
中文别名
——
英文名称
3-Allyl-2-methyl-cyclopent-2-enol
英文别名
2-Methyl-3-(prop-2-en-1-yl)cyclopent-2-en-1-ol;2-methyl-3-prop-2-enylcyclopent-2-en-1-ol
3-Allyl-2-methyl-cyclopent-2-enol化学式
CAS
645421-44-9
化学式
C9H14O
mdl
——
分子量
138.21
InChiKey
WTYFYXUJMOBCOC-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):
    1.2
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

上下游信息

  • 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:
    3-Allyl-2-methyl-cyclopent-2-enol 、 alkaline earth salt of/the/ methylsulfuric acid 生成 Pent-4-enoic acid 3-allyl-2-methyl-cyclopent-2-enyl ester
    参考文献:
    名称:
    A sequential Claisen/ring-closing metathesis approach to the synthesis of spirocyclic cyclopentanes and cyclohexanes
    摘要:
    A new method for the formation of spirocycles is described using a sequential Ireland-Claisen/Metathesis strategy to construct spirocyclic systems. Optimization of the Ireland-Claisen conditions provides the key metathesis substrates. The metathesis reactions were highly regioselective by virtue of steric hindrance in the substrate olefins. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.09.190
  • 作为产物:
    描述:
    3-Allyl-2-methyl-cyclopent-2-enone 在 sodium tetrahydroborate 、 cerium(III) chloride 作用下, 生成 3-Allyl-2-methyl-cyclopent-2-enol
    参考文献:
    名称:
    A sequential Claisen/ring-closing metathesis approach to the synthesis of spirocyclic cyclopentanes and cyclohexanes
    摘要:
    A new method for the formation of spirocycles is described using a sequential Ireland-Claisen/Metathesis strategy to construct spirocyclic systems. Optimization of the Ireland-Claisen conditions provides the key metathesis substrates. The metathesis reactions were highly regioselective by virtue of steric hindrance in the substrate olefins. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.09.190
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文献信息

  • Nouveaux éthers dont les restes organiques comportent des atomes chiraux, leur procédé de préparation et leur application au dédoublement des alcools, des phénols ou de certains composés de structure lactonique
    申请人:ROUSSEL-UCLAF
    公开号:EP0004493B1
    公开(公告)日:1981-05-06
  • A sequential Claisen/ring-closing metathesis approach to the synthesis of spirocyclic cyclopentanes and cyclohexanes
    作者:Patrick Beaulieu、William W. Ogilvie
    DOI:10.1016/j.tetlet.2003.09.190
    日期:2003.12
    A new method for the formation of spirocycles is described using a sequential Ireland-Claisen/Metathesis strategy to construct spirocyclic systems. Optimization of the Ireland-Claisen conditions provides the key metathesis substrates. The metathesis reactions were highly regioselective by virtue of steric hindrance in the substrate olefins. (C) 2003 Elsevier Ltd. All rights reserved.
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