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2-oxo-2-(pyren-3-yl)ethyl 2-phenylacetate | 1262722-93-9

中文名称
——
中文别名
——
英文名称
2-oxo-2-(pyren-3-yl)ethyl 2-phenylacetate
英文别名
(2-Oxo-2-pyren-1-ylethyl) 2-phenylacetate;(2-oxo-2-pyren-1-ylethyl) 2-phenylacetate
2-oxo-2-(pyren-3-yl)ethyl 2-phenylacetate化学式
CAS
1262722-93-9
化学式
C26H18O3
mdl
——
分子量
378.427
InChiKey
PDMFWKOYKZHNAG-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):
    6.2
  • 重原子数:
    29
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    2-oxo-2-(pyren-3-yl)ethyl 2-phenylacetate 作用下, 以 乙腈 为溶剂, 反应 0.2h, 生成 苯乙酸1-(hydroxyacetyl)pyrene
    参考文献:
    名称:
    1-Acetylpyrene with dual functions as an environment-sensitive fluorophore and fluorescent photoremovable protecting group
    摘要:
    A series of new fluorescent ester conjugates of carboxylic acids including amino acids was synthesized by coupling with an environment-sensitive fluorophore 1-acetylpyrene. Interestingly, the fluorescence properties of the ester conjugates and 1-acetylpyrene were found to be highly sensitive to its surrounding environment. The results obtained from the photolysis of the ester conjugates indicated that various factors like solvent, irradiation wavelength, and the structure of the conjugates govern the rate of the photocleavage. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.10.090
  • 作为产物:
    描述:
    苯乙酸1-(溴乙酰)芘potassium carbonate 、 potassium iodide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 10.0h, 以80%的产率得到2-oxo-2-(pyren-3-yl)ethyl 2-phenylacetate
    参考文献:
    名称:
    1-Acetylpyrene with dual functions as an environment-sensitive fluorophore and fluorescent photoremovable protecting group
    摘要:
    A series of new fluorescent ester conjugates of carboxylic acids including amino acids was synthesized by coupling with an environment-sensitive fluorophore 1-acetylpyrene. Interestingly, the fluorescence properties of the ester conjugates and 1-acetylpyrene were found to be highly sensitive to its surrounding environment. The results obtained from the photolysis of the ester conjugates indicated that various factors like solvent, irradiation wavelength, and the structure of the conjugates govern the rate of the photocleavage. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.10.090
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文献信息

  • 1-Acetylpyrene with dual functions as an environment-sensitive fluorophore and fluorescent photoremovable protecting group
    作者:Avijit Jana、Sanghamitra Atta、Sujan K. Sarkar、N.D. Pradeep Singh
    DOI:10.1016/j.tet.2010.10.090
    日期:2010.12
    A series of new fluorescent ester conjugates of carboxylic acids including amino acids was synthesized by coupling with an environment-sensitive fluorophore 1-acetylpyrene. Interestingly, the fluorescence properties of the ester conjugates and 1-acetylpyrene were found to be highly sensitive to its surrounding environment. The results obtained from the photolysis of the ester conjugates indicated that various factors like solvent, irradiation wavelength, and the structure of the conjugates govern the rate of the photocleavage. (C) 2010 Elsevier Ltd. All rights reserved.
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