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甲基环癸烷 | 13151-43-4

中文名称
甲基环癸烷
中文别名
——
英文名称
methylcyclodecane
英文别名
Methylcyclodecan
甲基环癸烷化学式
CAS
13151-43-4
化学式
C11H22
mdl
——
分子量
154.296
InChiKey
WFWNFBYXZQJMFM-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:
    69-70 °C(Press: 4 Torr)
  • 密度:
    0.781±0.06 g/cm3(Predicted)
  • 保留指数:
    1195;1202

计算性质

  • 辛醇/水分配系数(LogP):
    5.8
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 海关编码:
    2902199090

反应信息

  • 作为产物:
    描述:
    Cyclodecylmethyl-trimethyl-ammonium; hydroxide 生成 甲基环癸烷
    参考文献:
    名称:
    Amine Oxides. VIII. Medium-sized Cyclic Olefins from Amine Oxides and Quaternary Ammonium Hydroxides1,2
    摘要:
    Thermal decompositions of the N-oxides derived from N,N-dimethyl-1-methylcycloalk,lamines II having eight-, nine- and ten-membered rings yield olefin mixtures containing 98.6, 94.0 and 97.5%, respectively, of 1-methylcycloalkenes. Considerable amounts of the trans isomers are formed from the nine- and ten-membered N-oxides. Pyrolyses of the corresponding quaternary hydroxides produce mixtures of methylenecycloalkanes and 1-methylcycloalkenes (predominantly cis), violation of the Hofmann rule being at a maximum in the decomposition of the nine-membered quaternary hydroxide. Importance of relative product stabilities and the operation of non-bonded interactions are discussed as possible explanations for the observed directions of elimination. Thermal decompositions of the N-oxides and quaternary hydroxides of dimethylcycloalkvimethylamines IV containing eight-, nine- and ten-membered rings proceed as expected with formation of the corresponding methylenecycloalkanes.
    DOI:
    10.1021/ja01502a053
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文献信息

  • LEVASHOVA, T. V.;SEMEJKIN, O. V.;BELENKOVA, E. S., BECTH. MGU. XIMIYA, 1981, 22, N 6, 587-590
    作者:LEVASHOVA, T. V.、SEMEJKIN, O. V.、BELENKOVA, E. S.
    DOI:——
    日期:——
  • Amine Oxides. VIII. Medium-sized Cyclic Olefins from Amine Oxides and Quaternary Ammonium Hydroxides<sup>1,2</sup>
    作者:Arthur C. Cope、Engelbert Ciganek、Charles F. Howell、Edward E. Schweizer
    DOI:10.1021/ja01502a053
    日期:1960.9
    Thermal decompositions of the N-oxides derived from N,N-dimethyl-1-methylcycloalk,lamines II having eight-, nine- and ten-membered rings yield olefin mixtures containing 98.6, 94.0 and 97.5%, respectively, of 1-methylcycloalkenes. Considerable amounts of the trans isomers are formed from the nine- and ten-membered N-oxides. Pyrolyses of the corresponding quaternary hydroxides produce mixtures of methylenecycloalkanes and 1-methylcycloalkenes (predominantly cis), violation of the Hofmann rule being at a maximum in the decomposition of the nine-membered quaternary hydroxide. Importance of relative product stabilities and the operation of non-bonded interactions are discussed as possible explanations for the observed directions of elimination. Thermal decompositions of the N-oxides and quaternary hydroxides of dimethylcycloalkvimethylamines IV containing eight-, nine- and ten-membered rings proceed as expected with formation of the corresponding methylenecycloalkanes.
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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