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N-(3,5-dimethylphenyl)-7-ethylindole

中文名称
——
中文别名
——
英文名称
N-(3,5-dimethylphenyl)-7-ethylindole
英文别名
1-(3,5-Dimethylphenyl)-7-ethylindole
N-(3,5-dimethylphenyl)-7-ethylindole化学式
CAS
——
化学式
C18H19N
mdl
——
分子量
249.356
InChiKey
AHYPQOSFPPSYPI-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):
    5.2
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    4.9
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    7-乙基吲哚3,5-二甲基溴苯 在 tris(dibenzylideneacetone)dipalladium (0) 、 sodium t-butanolate1-[2-(di-tert-butylphosphino)phenyl]naphthalene 作用下, 以 甲苯 为溶剂, 生成 N-(3,5-dimethylphenyl)-7-ethylindole
    参考文献:
    名称:
    Efficient Palladium-Catalyzed N-Arylation of Indoles
    摘要:
    The N-arylation of indoles, including a variety of substituted ones, has been carried out using bulky, electron rich phosphines as the supporting ligand in combination with Pd-2(dba)(3). Using this catalyst system, the efficient coupling of indole and a variety of substituted indoles with aryl iodides, bromides, chlorides, and triflates can be achieved.
    DOI:
    10.1021/ol005728z
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文献信息

  • LIGANDS FOR METALS AND METAL-CATALYZED PROCESSES
    申请人:MASSACHUSETTS INSTITUTE OF TECHNOLOGY
    公开号:EP1097158B1
    公开(公告)日:2006-01-25
  • Ligands for metals and improved metal-catalyzed processes based thereon
    申请人:Massachussetts Institute of Technology
    公开号:EP1354887B1
    公开(公告)日:2007-04-25
  • [EN] LIGANDS FOR METALS AND IMPROVED METAL-CATALYZED PROCESSES BASED THEREON<br/>[FR] LIGANDS POUR METAUX ET PROCESSUS PERFECTIONNES CATALYSES PAR DES METAUX BASES SUR CEUX-CI
    申请人:MASSACHUSETTS INST TECHNOLOGY
    公开号:WO2000002887A2
    公开(公告)日:2000-01-20
    One aspect of the present invention relates to novel ligands for transition metals. A second aspect of the present invention relates to the use of catalysts comprising these ligands in transition metal-catalyzed carbon-heteroatom and carbon-carbon bond-forming reactions. The subject processes provide improvements in many features of the transition metal-catalyzed reactions, including the range of suitable substrates, reaction conditions, and efficiency.
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