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4,5-bis[4-(diphenylamino)phenyl]-2,7-di-tert-butyl-9,9-dimethyl-9H-xanthene | 1332869-93-8

中文名称
——
中文别名
——
英文名称
4,5-bis[4-(diphenylamino)phenyl]-2,7-di-tert-butyl-9,9-dimethyl-9H-xanthene
英文别名
——
4,5-bis[4-(diphenylamino)phenyl]-2,7-di-tert-butyl-9,9-dimethyl-9H-xanthene化学式
CAS
1332869-93-8
化学式
C59H56N2O
mdl
——
分子量
809.106
InChiKey
AJLVQMGSAFJNSM-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):
    16.99
  • 重原子数:
    62.0
  • 可旋转键数:
    8.0
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    15.71
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    参考文献:
    名称:
    Double-coupling of dibromo arenes with aryltriolborates for synthesis of diaryl-substituted planar frameworks
    摘要:
    A new method for simple and practical synthesis of diaryl-substituted arenes using potassium aryltriolborates was developed. Double-cross-coupling of dibromo arenes with aryltriolborates was carried out in the presence of a palladium catalyst, such as Pd(OAc)(2), Pd(PPh3)(4) or Pd(OAc)(2)/BIPHEP. The use of CuCl (40 mol %) with a palladium catalyst was found to be highly effective to give diaryl-substituted aromatic compounds in good yields. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.06.083
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文献信息

  • Double-coupling of dibromo arenes with aryltriolborates for synthesis of diaryl-substituted planar frameworks
    作者:Gao-Qiang Li、Yasunori Yamamoto、Norio Miyaura
    DOI:10.1016/j.tet.2011.06.083
    日期:2011.9
    A new method for simple and practical synthesis of diaryl-substituted arenes using potassium aryltriolborates was developed. Double-cross-coupling of dibromo arenes with aryltriolborates was carried out in the presence of a palladium catalyst, such as Pd(OAc)(2), Pd(PPh3)(4) or Pd(OAc)(2)/BIPHEP. The use of CuCl (40 mol %) with a palladium catalyst was found to be highly effective to give diaryl-substituted aromatic compounds in good yields. (C) 2011 Elsevier Ltd. All rights reserved.
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