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10-(2-hydroxyphenyl)-7-mesityl-10b-phenyl-10bH-11-oxa-4b1,10a-diaza-10bl4-boracyclopenta[e]aceanthrylen-10a-ium | 1171817-76-7

中文名称
——
中文别名
——
英文名称
10-(2-hydroxyphenyl)-7-mesityl-10b-phenyl-10bH-11-oxa-4b1,10a-diaza-10bl4-boracyclopenta[e]aceanthrylen-10a-ium
英文别名
——
10-(2-hydroxyphenyl)-7-mesityl-10b-phenyl-10bH-11-oxa-4b1,10a-diaza-10bl4-boracyclopenta[e]aceanthrylen-10a-ium化学式
CAS
1171817-76-7
化学式
C36H29BN2O2
mdl
——
分子量
532.449
InChiKey
OYOCIDTWZVNKSH-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:
    Convenient and highly efficient synthesis of boron–dipyrrins bearing an arylboronate center
    摘要:
    Novel boron-dipyrrins bearing an aryl group and a phenyloxy group linked directly to the boron center have been prepared in high yields from arylboronic acid. The unique Coordination geometry around the boron was determined by an X-ray crystallographic analysis. The complexes showed a strong fluorescence, and alkylation of the OH group shifted the emission to a longer wavelength with a larger Stokes shift.
    DOI:
    10.1016/j.tetlet.2009.02.094
  • 作为产物:
    描述:
    (mesityl)C((C4H2N)(C6H4)OH)((C4H3N)(C6H4)OH) 、 苯硼酸氯仿 为溶剂, 反应 3.0h, 以100%的产率得到10-(2-hydroxyphenyl)-7-mesityl-10b-phenyl-10bH-11-oxa-4b1,10a-diaza-10bl4-boracyclopenta[e]aceanthrylen-10a-ium
    参考文献:
    名称:
    Convenient and highly efficient synthesis of boron–dipyrrins bearing an arylboronate center
    摘要:
    Novel boron-dipyrrins bearing an aryl group and a phenyloxy group linked directly to the boron center have been prepared in high yields from arylboronic acid. The unique Coordination geometry around the boron was determined by an X-ray crystallographic analysis. The complexes showed a strong fluorescence, and alkylation of the OH group shifted the emission to a longer wavelength with a larger Stokes shift.
    DOI:
    10.1016/j.tetlet.2009.02.094
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文献信息

  • Convenient and highly efficient synthesis of boron–dipyrrins bearing an arylboronate center
    作者:Chusaku Ikeda、Tetsuji Maruyama、Tatsuya Nabeshima
    DOI:10.1016/j.tetlet.2009.02.094
    日期:2009.7
    Novel boron-dipyrrins bearing an aryl group and a phenyloxy group linked directly to the boron center have been prepared in high yields from arylboronic acid. The unique Coordination geometry around the boron was determined by an X-ray crystallographic analysis. The complexes showed a strong fluorescence, and alkylation of the OH group shifted the emission to a longer wavelength with a larger Stokes shift.
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