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3-Methylhex-3-en-1-yne | 62839-54-7

中文名称
——
中文别名
——
英文名称
3-Methylhex-3-en-1-yne
英文别名
——
3-Methylhex-3-en-1-yne化学式
CAS
62839-54-7
化学式
C7H10
mdl
——
分子量
94.1564
InChiKey
KYOGSVAQRNIVQL-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

物化性质

  • 沸点:
    93 °C
  • 密度:
    0.7671 g/cm3(Temp: 18 °C)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

SDS

SDS:3843f9b1f8741cc9f709a7cac9549d03
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反应信息

  • 作为反应物:
    描述:
    3-Methylhex-3-en-1-yne异丁醛苄胺copper(l) chloride 作用下, 以 乙酸乙酯 为溶剂, 反应 12.0h, 以80%的产率得到
    参考文献:
    名称:
    A3-Coupling Reaction as a Strategy Towards the Synthesis of Alkaloids
    摘要:
    A number of aldehydes, alkynols and benzylamines were submitted to A(3)-coupling reaction, under CuCl catalysis, giving strategically functionalized hydroxy-propargylamines. The procedure allows the use of alkyl as well as aryl aldehydes. Representative substrates were converted into five- and six-membered cyclic alkaloids by sequential one-pot N-debenzylation/triple bond reduction promoted by Pd, followed by a Mitsunobu-type cyclization.
    DOI:
    10.5935/0103-5053.20140223
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文献信息

  • A<sup>3</sup>-Coupling Reaction as a Strategy Towards the Synthesis of Alkaloids
    作者:Rafaela C. Carmona、Edison P. Wendler、George H. Sakae、João V. Comasseto、Alcindo A. Dos Santos
    DOI:10.5935/0103-5053.20140223
    日期:——
    A number of aldehydes, alkynols and benzylamines were submitted to A(3)-coupling reaction, under CuCl catalysis, giving strategically functionalized hydroxy-propargylamines. The procedure allows the use of alkyl as well as aryl aldehydes. Representative substrates were converted into five- and six-membered cyclic alkaloids by sequential one-pot N-debenzylation/triple bond reduction promoted by Pd, followed by a Mitsunobu-type cyclization.
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