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dimethyl 2-(5-methylhexa-2,3-dienyl)malonate | 1204503-45-6

中文名称
——
中文别名
——
英文名称
dimethyl 2-(5-methylhexa-2,3-dienyl)malonate
英文别名
——
dimethyl 2-(5-methylhexa-2,3-dienyl)malonate化学式
CAS
1204503-45-6
化学式
C12H18O4
mdl
——
分子量
226.273
InChiKey
VIVFQKNQHNNIKD-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):
    1.9
  • 重原子数:
    16
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    dimethyl 2-ethynylcyclopropane-1,1-dicarboxylate异丙基溴化镁copper(l) cyanide 作用下, 以 乙醚 为溶剂, 以82%的产率得到dimethyl 2-(5-methylhexa-2,3-dienyl)malonate
    参考文献:
    名称:
    Synthesis of Enantioenriched Allenes from 1,1-Cyclopropanediesters
    摘要:
    Highly substituted allenes were obtained by the S(N)2' addition of organocuprate reagents on 2-propargyl-1,1-cyclopropanediesters. This new methodology permits the synthesis of highly enantioenriched allenes as the reaction proceeds with retention of the enantiomeric purity of the starting cyclopropane. The use of higher order cuprates was instrumental in obtaining the reported results.
    DOI:
    10.1021/ol902766f
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文献信息

  • Iron-catalyzed addition of Grignard reagents to activated vinyl cyclopropanes
    作者:Benjamin D. Sherry、Alois Fürstner
    DOI:10.1039/b918818e
    日期:——
    A highly regioselective iron-catalyzed addition of branched primary, secondary or tertiary alkyl Grignard reagents to activated vinyl cyclopropanes is described, which likely proceeds by a direct addition mechanism as opposed to single electron transfer or an iron-allyl based process.
    描述了高区域选择性的铁催化的支链伯,仲或叔烷基格氏试剂向活化的乙烯基环丙烷的加成反应,其可能通过直接加成机理而不是单电子转移或基于铁-烯丙基的方法进行。
  • Synthesis of Enantioenriched Allenes from 1,1-Cyclopropanediesters
    作者:Pascal Cérat、Philipp J. Gritsch、Sébastien R. Goudreau、André B. Charette
    DOI:10.1021/ol902766f
    日期:2010.2.5
    Highly substituted allenes were obtained by the S(N)2' addition of organocuprate reagents on 2-propargyl-1,1-cyclopropanediesters. This new methodology permits the synthesis of highly enantioenriched allenes as the reaction proceeds with retention of the enantiomeric purity of the starting cyclopropane. The use of higher order cuprates was instrumental in obtaining the reported results.
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