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4,4-difluoro-1-iodo-2,6-dimethyl-3,5-(thien-2-yl)-4-bora-3a,4a-diaza-s-indacene | 1403582-79-5

中文名称
——
中文别名
——
英文名称
4,4-difluoro-1-iodo-2,6-dimethyl-3,5-(thien-2-yl)-4-bora-3a,4a-diaza-s-indacene
英文别名
——
4,4-difluoro-1-iodo-2,6-dimethyl-3,5-(thien-2-yl)-4-bora-3a,4a-diaza-s-indacene化学式
CAS
1403582-79-5
化学式
C19H14BF2IN2S2
mdl
——
分子量
510.178
InChiKey
OZTVZFTVUZXGFX-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:
    描述:
    5-trimethylstannyl-5'-hexyl-2,2'-bithiophene4,4-difluoro-1-iodo-2,6-dimethyl-3,5-(thien-2-yl)-4-bora-3a,4a-diaza-s-indacene四(三苯基膦)钯 作用下, 以 四氢呋喃 为溶剂, 反应 18.0h, 以76%的产率得到4,4-difluoro-1-(5’-hexyl-2,2’-bithien-5-yl)-2,6-dimethyl-3,5-(thien-2-yl)-4-bora-3a,4a-diaza-s-indacene
    参考文献:
    名称:
    Oligothienyl-BODIPYs: Red and Near-Infrared Emitters
    摘要:
    The synthesis of unsymmetrical 3,5-dioligothienyl-BODIPY derivatives and their optical and redox properties are reported. The key step is the monobromination of the 2,6-dimethyl-3,5-dithienyl-BODIPY at the a position of the thiophene moiety. The additional thiophene modules are attached by palladium-catalyzed cross-coupling reactions. Increasing the number of modules on each side of the BODIPY core progressively shifts the absorption to 677 nm and the emission to 769 nm.
    DOI:
    10.1021/ol302710z
  • 作为产物:
    描述:
    4,4′-difluoro-2,6-dimethyl-3,5-(dithien-2-yl)-4-bora-3a,4a-diaza-s-indacene一氯化碘 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 以32%的产率得到4,4-difluoro-1-iodo-2,6-dimethyl-3,5-(thien-2-yl)-4-bora-3a,4a-diaza-s-indacene
    参考文献:
    名称:
    Oligothienyl-BODIPYs: Red and Near-Infrared Emitters
    摘要:
    The synthesis of unsymmetrical 3,5-dioligothienyl-BODIPY derivatives and their optical and redox properties are reported. The key step is the monobromination of the 2,6-dimethyl-3,5-dithienyl-BODIPY at the a position of the thiophene moiety. The additional thiophene modules are attached by palladium-catalyzed cross-coupling reactions. Increasing the number of modules on each side of the BODIPY core progressively shifts the absorption to 677 nm and the emission to 769 nm.
    DOI:
    10.1021/ol302710z
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