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(7-甲氧基香豆素-4-基)甲基甲磺酸酯 | 84447-28-9

中文名称
(7-甲氧基香豆素-4-基)甲基甲磺酸酯
中文别名
——
英文名称
(7-methoxycoumarin-4-yl)methylmethanesulfonate
英文别名
(7-Methoxy-2-oxochromen-4-yl)methyl methanesulfonate
(7-甲氧基香豆素-4-基)甲基甲磺酸酯化学式
CAS
84447-28-9
化学式
C12H12O6S
mdl
——
分子量
284.29
InChiKey
XUPCPJDOGXOUPP-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

  • 熔点:
    159 °C
  • 沸点:
    513.5±50.0 °C(Predicted)
  • 密度:
    1.393±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    87.3
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (7-甲氧基香豆素-4-基)甲基甲磺酸酯 在 HEPES buffer 作用下, 以 乙腈 为溶剂, 生成 甲烷磺酸4-(hydroxymethyl)-7-methoxycoumarin
    参考文献:
    名称:
    Deactivation Behavior and Excited-State Properties of (Coumarin-4-yl)methyl Derivatives. 1. Photocleavage of (7-Methoxycoumarin-4-yl)methyl-Caged Acids with Fluorescence Enhancement
    摘要:
    The photochemistry of the (7-methoxycoumarin-4-yl)methyl (MCM) carboxylates 3a-d, the mesylate 4, and the phosphates 5a-e has been examined under near physiological conditions in acetonitrile or methanol/aqueous HEPES buffer solution, respectively Analysis of photoproducts as well as measurements of photochemical quantum yields, fluorescence quantum yields, and lifetimes for the excited singlet state verified the similar photochemical and photophysical behavior of all the esters studied here. 4-(Hydroxymethyl)-7-methoxycoumarin (2) and the corresponding free acids were obtained as major products upon irradiation. The rates of deactivation of the excited MCM derivatives 3a-5e were found to be dependent on the:leaving group ability of the anion concerned as well as on the solvent polarity. The polarity dependence and the exclusive formation of O-18-labeled 2 during irradiation of 5a in O-18-labeled water indicate that photocleavage of the excited singlet state of the MCM caged compounds 3a-5e proceeds via a photo S(N)1 mechanism (solvent-assisted photoheterolysis).
    DOI:
    10.1021/jo9910233
  • 作为产物:
    描述:
    7-甲氧基香豆素-4-腙 在 magnesium sulfate 、 silver(l) oxide 作用下, 以 氯仿 为溶剂, 反应 6.0h, 生成 (7-甲氧基香豆素-4-基)甲基甲磺酸酯
    参考文献:
    名称:
    Ito, Keiichi; Sawanobori, Junko, Synthetic Communications, 1982, vol. 12, # 9, p. 665 - 672
    摘要:
    DOI:
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文献信息

  • ITO, KEIICHI;SAWANOBORI, JUNKO, SYNTH. COMMUN., 1982, 12, N 9, 665-671
    作者:ITO, KEIICHI、SAWANOBORI, JUNKO
    DOI:——
    日期:——
  • Deactivation Behavior and Excited-State Properties of (Coumarin-4-yl)methyl Derivatives. 1. Photocleavage of (7-Methoxycoumarin-4-yl)methyl-Caged Acids with Fluorescence Enhancement
    作者:Björn Schade、Volker Hagen、Reinhard Schmidt、Ralph Herbrich、Eberhard Krause、Torsten Eckardt、Jürgen Bendig
    DOI:10.1021/jo9910233
    日期:1999.12.1
    The photochemistry of the (7-methoxycoumarin-4-yl)methyl (MCM) carboxylates 3a-d, the mesylate 4, and the phosphates 5a-e has been examined under near physiological conditions in acetonitrile or methanol/aqueous HEPES buffer solution, respectively Analysis of photoproducts as well as measurements of photochemical quantum yields, fluorescence quantum yields, and lifetimes for the excited singlet state verified the similar photochemical and photophysical behavior of all the esters studied here. 4-(Hydroxymethyl)-7-methoxycoumarin (2) and the corresponding free acids were obtained as major products upon irradiation. The rates of deactivation of the excited MCM derivatives 3a-5e were found to be dependent on the:leaving group ability of the anion concerned as well as on the solvent polarity. The polarity dependence and the exclusive formation of O-18-labeled 2 during irradiation of 5a in O-18-labeled water indicate that photocleavage of the excited singlet state of the MCM caged compounds 3a-5e proceeds via a photo S(N)1 mechanism (solvent-assisted photoheterolysis).
  • Ito, Keiichi; Sawanobori, Junko, Synthetic Communications, 1982, vol. 12, # 9, p. 665 - 672
    作者:Ito, Keiichi、Sawanobori, Junko
    DOI:——
    日期:——
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