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6-环己基-3-甲基-1,4-二氧杂螺[4.5]癸烷 | 62674-05-9

中文名称
6-环己基-3-甲基-1,4-二氧杂螺[4.5]癸烷
中文别名
——
英文名称
2-methyl-6-cyclohexyl-1,4-dioxaspiro[4.5]decane
英文别名
6-cyclohexyl-2-methyl-1,4-dioxa-spiro[4.5]decane;6-Cyclohexyl-2-methyl-1,4-dioxaspiro[4.5]decane;6-cyclohexyl-3-methyl-1,4-dioxaspiro[4.5]decane
6-环己基-3-甲基-1,4-二氧杂螺[4.5]癸烷化学式
CAS
62674-05-9
化学式
C15H26O2
mdl
——
分子量
238.37
InChiKey
NOBYDUIBJRUEAP-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:
    150-152 °C(Press: 1.2 Torr)
  • 密度:
    1.0541 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:72f9aa0c7c912c60dd990e2af6a6d7dc
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反应信息

  • 作为产物:
    描述:
    1,2-丙二醇2-环己基环己酮 在 P0.17Mo2.4CoBr0.27O6.8 作用下, 以 5,5-dimethyl-1,3-cyclohexadiene 为溶剂, 以79%的产率得到6-环己基-3-甲基-1,4-二氧杂螺[4.5]癸烷
    参考文献:
    名称:
    Synthesis of higher spiroacetals by condensation of alkyl- and cycloalkylcyclopentanones and cyclohexanones with dihydric alcohols in the presence of heterogenic catalysts
    摘要:
    The condensation of C-3-C-7 alkyl- and cycloalkylcyclopentanones and cyclohexanones with 1,2-ethane-, 1,2-propane-, and 1,3-butanediols in the presence of heterogenic acid catalysts provided new representatives of spiroacetals. The highest yields of reaction products were obtained in the presence of phosphomolybdic heteropolyacid additionally modified with cobalt and bromine, and also in the presence of the chlorinated cationite KU-23 at 110-130A degrees C. The synthesized spiroacetals possess the jasmine and menthol-wooden fragrance of various tinges.
    DOI:
    10.1134/s1070428011080069
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文献信息

  • Synthesis of higher spiroacetals by condensation of alkyl- and cycloalkylcyclopentanones and cyclohexanones with dihydric alcohols in the presence of heterogenic catalysts
    作者:Kh. M. Alimardanov、O. A. Sadygov、M. F. Abbasov、E. T. Suleimanova、N. A. Dzhafarova、M. Ya. Abdullaeva、S. M. Abbasova
    DOI:10.1134/s1070428011080069
    日期:2011.8
    The condensation of C-3-C-7 alkyl- and cycloalkylcyclopentanones and cyclohexanones with 1,2-ethane-, 1,2-propane-, and 1,3-butanediols in the presence of heterogenic acid catalysts provided new representatives of spiroacetals. The highest yields of reaction products were obtained in the presence of phosphomolybdic heteropolyacid additionally modified with cobalt and bromine, and also in the presence of the chlorinated cationite KU-23 at 110-130A degrees C. The synthesized spiroacetals possess the jasmine and menthol-wooden fragrance of various tinges.
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