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diethyl (S)-5-{2-[(2,2,2-trifluoro-1-methoxyethyl)phenyl]}-2,3,7,8-tetramethyl-10H-dipyrrin-1,9-dicarboxylate | 670247-24-2

中文名称
——
中文别名
——
英文名称
diethyl (S)-5-{2-[(2,2,2-trifluoro-1-methoxyethyl)phenyl]}-2,3,7,8-tetramethyl-10H-dipyrrin-1,9-dicarboxylate
英文别名
——
diethyl (S)-5-{2-[(2,2,2-trifluoro-1-methoxyethyl)phenyl]}-2,3,7,8-tetramethyl-10H-dipyrrin-1,9-dicarboxylate化学式
CAS
670247-24-2
化学式
C28H31F3N2O5
mdl
——
分子量
532.56
InChiKey
HPXSAQDXVRYCAF-FVRDZJJLSA-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):
    6.17
  • 重原子数:
    38.0
  • 可旋转键数:
    8.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    89.98
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    diethyl (S)-5-{2-[(2,2,2-trifluoro-1-methoxyethyl)phenyl]}-2,3,7,8-tetramethyl-10H-dipyrrin-1,9-dicarboxylate三氟化硼乙醚N,N-二异丙基乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 0.83h, 以77%的产率得到diethyl (S)-5-{2-[(2,2,2-trifluoro-1-methoxyethyl)phenyl]}-1,2,6,7-tetramethyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene-3,5-dicarboxylate
    参考文献:
    名称:
    Synthesis, Chiroptical Properties, and Solid-State Structure Determination of Two New Chiral Dipyrrin Difluoroboryl Chelates
    摘要:
    Two new types of optically active BODIPY fluorophores bearing chiral phenyl substituents either at the meso-position or at both external alpha-positions have been synthesized. Their chiroptical properties are strongly dependent both on the position of the chiral group and on the protonation of the chromophore. The solid-state structures of one of the difluoroboryl chelates bearing the chiral phenyl substituent at the meso-position (9a) as well as of the corresponding ligand (8a) and its perchlorate have been determined by X-ray diffraction analysis. These are, to the best of our knowledge, the first crystal structures of a dipyrrin free base and of a dipyrrin salt which have been obtained by X-ray diffraction analysis. Hence, for the first time, the helical structure of a protonated dipyrrin chromophore has been proved experimentally.
    DOI:
    10.1021/ja030542r
  • 作为产物:
    参考文献:
    名称:
    Synthesis, Chiroptical Properties, and Solid-State Structure Determination of Two New Chiral Dipyrrin Difluoroboryl Chelates
    摘要:
    Two new types of optically active BODIPY fluorophores bearing chiral phenyl substituents either at the meso-position or at both external alpha-positions have been synthesized. Their chiroptical properties are strongly dependent both on the position of the chiral group and on the protonation of the chromophore. The solid-state structures of one of the difluoroboryl chelates bearing the chiral phenyl substituent at the meso-position (9a) as well as of the corresponding ligand (8a) and its perchlorate have been determined by X-ray diffraction analysis. These are, to the best of our knowledge, the first crystal structures of a dipyrrin free base and of a dipyrrin salt which have been obtained by X-ray diffraction analysis. Hence, for the first time, the helical structure of a protonated dipyrrin chromophore has been proved experimentally.
    DOI:
    10.1021/ja030542r
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