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N-(S)-2-dodecyloxy-1-methyl-2-oxoethyl-N'-(S)-3-methyl-1-(oxo(1H,1H,2H,2H-perfluorodecyloxy)ethyl)butyl-3,4,9,10-perylenetetracarboxyldiimide

中文名称
——
中文别名
——
英文名称
N-(S)-2-dodecyloxy-1-methyl-2-oxoethyl-N'-(S)-3-methyl-1-(oxo(1H,1H,2H,2H-perfluorodecyloxy)ethyl)butyl-3,4,9,10-perylenetetracarboxyldiimide
英文别名
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl (2S)-2-[18-[(2S)-1-dodecoxy-1-oxopropan-2-yl]-6,8,17,19-tetraoxo-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(23),2,4,9,11,13,15,20(24),21,25-decaen-7-yl]-4-methylpentanoate
N-(S)-2-dodecyloxy-1-methyl-2-oxoethyl-N'-(S)-3-methyl-1-(oxo(1H,1H,2H,2H-perfluorodecyloxy)ethyl)butyl-3,4,9,10-perylenetetracarboxyldiimide化学式
CAS
——
化学式
C55H51F17N2O8
mdl
——
分子量
1190.99
InChiKey
YNUZGFYWSDFRID-AIJWEMPKSA-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):
    17.4
  • 重原子数:
    82
  • 可旋转键数:
    28
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    127
  • 氢给体数:
    0
  • 氢受体数:
    25

反应信息

  • 作为产物:
    描述:
    N-(S)-1-carboxyethyl-N'-(S)-3-methyl-1-(oxo(1H,1H,2H,2H-perfluorodecyloxy)methyl)butyl-3,4,9,10-perylenetetracarboxyldiimide 、 溴代十二烷18-冠醚-6potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 以85%的产率得到N-(S)-2-dodecyloxy-1-methyl-2-oxoethyl-N'-(S)-3-methyl-1-(oxo(1H,1H,2H,2H-perfluorodecyloxy)ethyl)butyl-3,4,9,10-perylenetetracarboxyldiimide
    参考文献:
    名称:
    Facile synthesis of chiral unsymmetric perylene tetracarboxylic diimides involving α-amino acids
    摘要:
    A facile synthesis of chiral unsymmetric perylene tetracarboxylic diimides (PDIs) has been developed and the first two nonracemic chiral amphiphilic PDIs have been synthesized. The key building blocks, AB bifunctional 3,4,9, 10-perylenetetracarboxylic-3,4-anhydride-9, 10-imides, were prepared conveniently from enantiomerically pure alpha-amino acids, which were introduced as the steric and stereochemical controlling units. Such building blocks allow the incorporation of sterically and stereochemically controlled PDI moieties into both terminal and inner positions. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.07.099
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文献信息

  • Facile synthesis of chiral unsymmetric perylene tetracarboxylic diimides involving α-amino acids
    作者:Runkun Sun、Chenming Xue、Mariam Owak、Ralf M. Peetz、Shi Jin
    DOI:10.1016/j.tetlet.2007.07.099
    日期:2007.9
    A facile synthesis of chiral unsymmetric perylene tetracarboxylic diimides (PDIs) has been developed and the first two nonracemic chiral amphiphilic PDIs have been synthesized. The key building blocks, AB bifunctional 3,4,9, 10-perylenetetracarboxylic-3,4-anhydride-9, 10-imides, were prepared conveniently from enantiomerically pure alpha-amino acids, which were introduced as the steric and stereochemical controlling units. Such building blocks allow the incorporation of sterically and stereochemically controlled PDI moieties into both terminal and inner positions. (c) 2007 Elsevier Ltd. All rights reserved.
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