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| 1603829-39-5

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1603829-39-5
化学式
Br*C19H18NO2
mdl
——
分子量
372.261
InChiKey
JMWLCPIOHVXJGC-UHFFFAOYSA-M
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):
    0.33
  • 重原子数:
    23.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    30.18
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    正丁基锂四甲基乙二胺potassium carbonate 作用下, 以 四氢呋喃 为溶剂, 反应 5.25h, 生成 2-(6-methoxynaphthalen-2-yl)-5-(p-tolyl)indolizine
    参考文献:
    名称:
    Synthesis, photophysical, and electrochemical properties of 2,5-diaryl-indolizines
    摘要:
    A variety of novel 2,5-dialyl-indolizines have been prepared through the palladium-catalyzed cross-coupling reactions of organozinc reagents prepared from 2-aryl-indolizines with aromatic halides. The photophysical properties of representative compounds indicate that the 2,5-diaryl-indolizines are promising candidates to be used in optoelectronic devices and biomolecular labeling. In addition, cyclic voltammetry studies of some nitrophenyl-substituted indolizines have shown evidences of an oxidation process without the correspondent reduction peak suggesting a dimerization reaction. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.11.105
  • 作为产物:
    描述:
    碳酸甲丙酯2-(溴乙酰基)-6-甲氧基萘丙酮 为溶剂, 反应 4.0h, 生成
    参考文献:
    名称:
    Synthesis, photophysical, and electrochemical properties of 2,5-diaryl-indolizines
    摘要:
    A variety of novel 2,5-dialyl-indolizines have been prepared through the palladium-catalyzed cross-coupling reactions of organozinc reagents prepared from 2-aryl-indolizines with aromatic halides. The photophysical properties of representative compounds indicate that the 2,5-diaryl-indolizines are promising candidates to be used in optoelectronic devices and biomolecular labeling. In addition, cyclic voltammetry studies of some nitrophenyl-substituted indolizines have shown evidences of an oxidation process without the correspondent reduction peak suggesting a dimerization reaction. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2013.11.105
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