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4-Methyloxy-5-hexen-1-ol mesylate | 1027246-76-9

中文名称
——
中文别名
——
英文名称
4-Methyloxy-5-hexen-1-ol mesylate
英文别名
4-Methoxyhex-5-enyl methanesulfonate
4-Methyloxy-5-hexen-1-ol mesylate化学式
CAS
1027246-76-9
化学式
C8H16O4S
mdl
——
分子量
208.279
InChiKey
PPCNBVDAOGYTLA-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:
    322.6±35.0 °C(Predicted)
  • 密度:
    1.097±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    61
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-Methyloxy-5-hexen-1-ol mesylate偶氮二异丁腈三正丁基氢锡 、 sodium iodide 作用下, 以 丙酮 为溶剂, 反应 11.75h, 生成 环己基甲醚
    参考文献:
    名称:
    Cyclization of (4-Methoxy-5-hexenyl)lithium
    摘要:
    The cyclization of (4-methoxy-5-hexenyl)lithium (1), which was prepared by lithium-iodine exchange between 3-methoxy-6-iodo-1-hexene (2) and 1.75 molar equiv of t-BuLi in diethyl ether-n-pentane solution at -78 degrees C, has been investigated in a variety of solvent systems. The isomeric composition of the cis- and trans-1-methoxy-2-methylcyclopentane produced upon cyclization of 1 followed by quench with MeOH has been found to be dramatically dependent on the solvent system in which the isomerization is conducted.
    DOI:
    10.1021/jo00101a010
  • 作为产物:
    描述:
    6-<(Tetrahydropyran-2-yl)oxy>-1-hexen-3-ol盐酸 、 sodium hydride 、 三乙胺 作用下, 以 四氢呋喃乙醇二氯甲烷 为溶剂, 反应 1.5h, 生成 4-Methyloxy-5-hexen-1-ol mesylate
    参考文献:
    名称:
    Cyclization of (4-Methoxy-5-hexenyl)lithium
    摘要:
    The cyclization of (4-methoxy-5-hexenyl)lithium (1), which was prepared by lithium-iodine exchange between 3-methoxy-6-iodo-1-hexene (2) and 1.75 molar equiv of t-BuLi in diethyl ether-n-pentane solution at -78 degrees C, has been investigated in a variety of solvent systems. The isomeric composition of the cis- and trans-1-methoxy-2-methylcyclopentane produced upon cyclization of 1 followed by quench with MeOH has been found to be dramatically dependent on the solvent system in which the isomerization is conducted.
    DOI:
    10.1021/jo00101a010
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文献信息

  • Cyclization of (4-Methoxy-5-hexenyl)lithium
    作者:William F. Bailey、Xing-Long Jiang
    DOI:10.1021/jo00101a010
    日期:1994.11
    The cyclization of (4-methoxy-5-hexenyl)lithium (1), which was prepared by lithium-iodine exchange between 3-methoxy-6-iodo-1-hexene (2) and 1.75 molar equiv of t-BuLi in diethyl ether-n-pentane solution at -78 degrees C, has been investigated in a variety of solvent systems. The isomeric composition of the cis- and trans-1-methoxy-2-methylcyclopentane produced upon cyclization of 1 followed by quench with MeOH has been found to be dramatically dependent on the solvent system in which the isomerization is conducted.
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