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(7-methylindolizine-1,2,3-triyl)tris((4-bromophenyl)methanone) | 1352441-18-9

中文名称
——
中文别名
——
英文名称
(7-methylindolizine-1,2,3-triyl)tris((4-bromophenyl)methanone)
英文别名
[2,3-Bis(4-bromobenzoyl)-7-methylindolizin-1-yl]-(4-bromophenyl)methanone;[2,3-bis(4-bromobenzoyl)-7-methylindolizin-1-yl]-(4-bromophenyl)methanone
(7-methylindolizine-1,2,3-triyl)tris((4-bromophenyl)methanone)化学式
CAS
1352441-18-9
化学式
C30H18Br3NO3
mdl
——
分子量
680.19
InChiKey
XUEYXOKNFHINGF-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

物化性质

  • 熔点:
    215-216 °C
  • 密度:
    1.65±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    9.3
  • 重原子数:
    37
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.03
  • 拓扑面积:
    55.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-甲基吡啶2,4'-二溴苯乙酮哌啶 、 sodium carbonate 作用下, 以 乙腈 为溶剂, 反应 16.0h, 以40%的产率得到(7-methylindolizine-1,2,3-triyl)tris((4-bromophenyl)methanone)
    参考文献:
    名称:
    One-pot multicomponent synthesis of polysubstituted indolizines
    摘要:
    Concise and efficient four-component tandem approaches to polysubstituted indolizines have been developed under metal-free and mild aerobic conditions in refluxing acetonitrile. The mechanism of the novel reactions was proposed involving the formation of pyridinium ylides and alpha,beta-unsaturated ketones with subsequent 1,3-dipolar cycloaddition and aromatization reaction. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.10.083
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文献信息

  • One-pot multicomponent synthesis of polysubstituted indolizines
    作者:Zhenjun Mao、Xuejian Li、Xufeng Lin、Ping Lu、Yanguang Wang
    DOI:10.1016/j.tet.2011.10.083
    日期:2012.1
    Concise and efficient four-component tandem approaches to polysubstituted indolizines have been developed under metal-free and mild aerobic conditions in refluxing acetonitrile. The mechanism of the novel reactions was proposed involving the formation of pyridinium ylides and alpha,beta-unsaturated ketones with subsequent 1,3-dipolar cycloaddition and aromatization reaction. (C) 2011 Elsevier Ltd. All rights reserved.
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