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3-(hydroxymethyl)-3,5,5-trimethyl-1-pyrazoline | 38634-80-9

中文名称
——
中文别名
——
英文名称
3-(hydroxymethyl)-3,5,5-trimethyl-1-pyrazoline
英文别名
(3,5,5-trimethyl-4,5-dihydro-3H-pyrazol-3-yl)-methanol;3-Hydroxymethyl-3,5,5-trimethyl-1-pyrazolin;(3,5,5-Trimethyl-1-pyrazolin-3-yl)methanol;(3,5,5-trimethyl-4H-pyrazol-3-yl)methanol
3-(hydroxymethyl)-3,5,5-trimethyl-1-pyrazoline化学式
CAS
38634-80-9
化学式
C7H14N2O
mdl
——
分子量
142.201
InChiKey
UQOHJUGHNKUZBV-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:
    181.7±9.0 °C(Predicted)
  • 密度:
    1.08±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.37
  • 重原子数:
    10.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    44.95
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    4-苯甲酰基苯甲酰氯3-(hydroxymethyl)-3,5,5-trimethyl-1-pyrazoline吡啶 作用下, 以 氯仿 为溶剂, 反应 0.5h, 以44%的产率得到(3,5,5-trimethyl-1-pyrazolin-3-yl)methyl 4-benzoylbenzoate
    参考文献:
    名称:
    Intramolecular triplet energy transfer in ester-linked bichromophoric azoalkanes and naphthalenes
    摘要:
    The photophysics of a series of compounds has been studied wherein a triplet sensitizer such as benzophenone (BB) or thioxanthone (TH) is linked via an ester group to an azoalkane such as 3,3,5,5-tetramethyl-1-pyrazoline (PY) or 2,3-diazabicyclo-[2.2.2]oct-2-ene (DBO). The observation of phosphorescence from the sensitizer moiety in a frozen glass and triplet lifetime measurements in solution show that intramolecular triplet energy transfer (ET) can be remarkably slow. Model compounds in which naphthalene replaces the azo group behave normally, exhibiting complete and rapid intramolecular ET. Despite the small size of the azo group, its critical radius, R0, for intermolecular ET in a frozen glass is comparable to that of naphthalene. When the donor and azo chromophores are closely linked by alkyl groups, ET is very rapid. No phosphorescence or T-T absorption of the azo group could be detected, but quenching experiments show that the triplet lifetime of cyclic azoalkanes is much shorter than their singlet lifetime.
    DOI:
    10.1021/j100198a011
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