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3-Benzoyl-2-(4-methylphenyl)-5-phenylcyclopenta-2,4-diene-1,1-dicarbonitrile | 1010795-17-1

中文名称
——
中文别名
——
英文名称
3-Benzoyl-2-(4-methylphenyl)-5-phenylcyclopenta-2,4-diene-1,1-dicarbonitrile
英文别名
——
3-Benzoyl-2-(4-methylphenyl)-5-phenylcyclopenta-2,4-diene-1,1-dicarbonitrile化学式
CAS
1010795-17-1
化学式
C27H18N2O
mdl
——
分子量
386.453
InChiKey
AQWHYXHWQNYWJO-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):
    4.9
  • 重原子数:
    30
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    64.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-(4-甲基亚苄基)-丙二腈二苯甲酰基乙炔三苯基膦 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以72%的产率得到3-Benzoyl-2-(4-methylphenyl)-5-phenylcyclopenta-2,4-diene-1,1-dicarbonitrile
    参考文献:
    名称:
    Reaction between triphenylphosphine, diaroylacetylenes and arylidenemalononitriles: a novel and simple synthesis of 3-aroyl-2,5-diaryl-2,4-cyclopentadiene-1,1-dicarbonitriles
    摘要:
    A novel and simple synthesis of 3-aroyl-2,5-diaryl-2,4-cyclopentadiene-1,1-dicarbonitriles is described. The reactive 1:1 zwitterionic intermediate, formed by the addition of triphenylphosphine to diaroylacetylenes, was trapped by arylidenemalononitriles to produce the title compounds under mild reaction conditions in fairly good yields. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.12.018
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文献信息

  • Reaction between triphenylphosphine, diaroylacetylenes and arylidenemalononitriles: a novel and simple synthesis of 3-aroyl-2,5-diaryl-2,4-cyclopentadiene-1,1-dicarbonitriles
    作者:Mehdi Adib、Mohammad Hosein Sayahi、Shabnam Mahernia、Long-Guan Zhu
    DOI:10.1016/j.tetlet.2007.12.018
    日期:2008.2
    A novel and simple synthesis of 3-aroyl-2,5-diaryl-2,4-cyclopentadiene-1,1-dicarbonitriles is described. The reactive 1:1 zwitterionic intermediate, formed by the addition of triphenylphosphine to diaroylacetylenes, was trapped by arylidenemalononitriles to produce the title compounds under mild reaction conditions in fairly good yields. (c) 2007 Elsevier Ltd. All rights reserved.
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