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10-(3,5-bis(decyloxy)phenyl)-5,5-difluoro-1,3,7,9-tetramethyl-2,8-bis(pyridin-4-ylethynyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium | 1191301-54-8

中文名称
——
中文别名
——
英文名称
10-(3,5-bis(decyloxy)phenyl)-5,5-difluoro-1,3,7,9-tetramethyl-2,8-bis(pyridin-4-ylethynyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium
英文别名
——
10-(3,5-bis(decyloxy)phenyl)-5,5-difluoro-1,3,7,9-tetramethyl-2,8-bis(pyridin-4-ylethynyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium化学式
CAS
1191301-54-8
化学式
C53H65BF2N4O2
mdl
——
分子量
838.933
InChiKey
POCIRVIZWVBIIO-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Tetrastyryl-Bodipy Dyes: Convenient Synthesis and Characterization of Elusive Near IR Fluorophores
    摘要:
    1,3,5,7-Tetramethyl-Bodipy derivatives undergo Knoevenagel-type condensations with aromatic aldehydes to ultimately yield tetrastyryl-Bodipy derivatives. The resulting dyes absorb and emit strongly in the near IR. As the versatility of the Bodipy dyes are fully appreciated, these new tetrastyryl dyes are likely to be featured in a variety of functional supramolecular systems.
    DOI:
    10.1021/ol9019056
  • 作为产物:
    描述:
    4-乙炔基吡啶4,4-difluoro-8-[3',5'-bis(decyloxy)phenyl]-2,6-diiodo-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide二异丙胺 作用下, 以 四氢呋喃 为溶剂, 反应 24.0h, 以75%的产率得到10-(3,5-bis(decyloxy)phenyl)-5,5-difluoro-1,3,7,9-tetramethyl-2,8-bis(pyridin-4-ylethynyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium
    参考文献:
    名称:
    Tetrastyryl-Bodipy Dyes: Convenient Synthesis and Characterization of Elusive Near IR Fluorophores
    摘要:
    1,3,5,7-Tetramethyl-Bodipy derivatives undergo Knoevenagel-type condensations with aromatic aldehydes to ultimately yield tetrastyryl-Bodipy derivatives. The resulting dyes absorb and emit strongly in the near IR. As the versatility of the Bodipy dyes are fully appreciated, these new tetrastyryl dyes are likely to be featured in a variety of functional supramolecular systems.
    DOI:
    10.1021/ol9019056
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