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Isobutyl-Kation | 19252-54-1

中文名称
——
中文别名
——
英文名称
Isobutyl-Kation
英文别名
isobutyl cation;2-methylpropane
Isobutyl-Kation化学式
CAS
19252-54-1
化学式
C4H9
mdl
——
分子量
57.1155
InChiKey
DOXFILCLISGXIX-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):
    2.1
  • 重原子数:
    4
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

SDS

SDS:18ec65ea24fcb9e97691a630c9cba377
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Reaction of ammonia with accelerated benzoyl ions under multiple-collison conditions in a triple quadrupole instrument
    摘要:
    AbstractThe reaction of benzoyl ion with ammonia in multiple‐collision conditions in the second quadrupole assembly of a triple quadrupole mass spectrometer at (laboratory) ion kinetic energies from 0 to 20 eV produced the even‐electron ions [C6H5]+, [C6H5NH3·(NH3)m]+ (m = 0, 1) and [C6H5CONH3·(NH3)n]+ (n = 0, 1, 2, 3) and the odd‐electron ions [C6H4NH3·(NH3)p]+· (p = 0, 1). Thermochemical information could not be obtained under multiple‐collision conditions: both exothermic and endothermic reactions were observed, with no translational‐energy onset measurable for the endothermic processes, nor decrease in the yield of the exothermic processes at high energies. The behaviour of cluster‐ion intensities as pressure varied was qualitatively as expected. There are pressure and energy regions where spectra change little; if this feature were to be general, it would point to some utility for these conditions in qualitative analysis.
    DOI:
    10.1002/oms.1210220304
  • 作为产物:
    参考文献:
    名称:
    Proton affinities and photoelectron spectra of three-membered-ring heterocycles
    摘要:
    DOI:
    10.1021/ja00536a004
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文献信息

  • Methyl-substituted cyclopropylcarbinyl (alias vinyl-bridged ethylene) carbocations. Molecular orbital calculations and criteria for structure representation-nomenclature decisions
    作者:Lawrence R. Schmitz、Ted S. Sorensen
    DOI:10.1021/ja00373a045
    日期:1982.5
  • Proton affinities and photoelectron spectra of three-membered-ring heterocycles
    作者:Donald H. Aue、Hugh M. Webb、William R. Davidson、Mariano Vidal、Michael T. Bowers、Harold Goldwhite、Lawrence E. Vertal、John E. Douglas、Peter A. Kollman、George L. Kenyon
    DOI:10.1021/ja00536a004
    日期:1980.7
  • Reaction of ammonia with accelerated benzoyl ions under multiple-collison conditions in a triple quadrupole instrument
    作者:Earl L. White、Jean-Claude Tabet、Maurice M. Bursey
    DOI:10.1002/oms.1210220304
    日期:1987.3
    AbstractThe reaction of benzoyl ion with ammonia in multiple‐collision conditions in the second quadrupole assembly of a triple quadrupole mass spectrometer at (laboratory) ion kinetic energies from 0 to 20 eV produced the even‐electron ions [C6H5]+, [C6H5NH3·(NH3)m]+ (m = 0, 1) and [C6H5CONH3·(NH3)n]+ (n = 0, 1, 2, 3) and the odd‐electron ions [C6H4NH3·(NH3)p]+· (p = 0, 1). Thermochemical information could not be obtained under multiple‐collision conditions: both exothermic and endothermic reactions were observed, with no translational‐energy onset measurable for the endothermic processes, nor decrease in the yield of the exothermic processes at high energies. The behaviour of cluster‐ion intensities as pressure varied was qualitatively as expected. There are pressure and energy regions where spectra change little; if this feature were to be general, it would point to some utility for these conditions in qualitative analysis.
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