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1-(5-methyl-4'-nitrobiphenyl-2-yl)ethanone | 1233011-60-3

中文名称
——
中文别名
——
英文名称
1-(5-methyl-4'-nitrobiphenyl-2-yl)ethanone
英文别名
1-[4-Methyl-2-(4-nitrophenyl)phenyl]ethanone;1-[4-methyl-2-(4-nitrophenyl)phenyl]ethanone
1-(5-methyl-4'-nitrobiphenyl-2-yl)ethanone化学式
CAS
1233011-60-3
化学式
C15H13NO3
mdl
——
分子量
255.273
InChiKey
QAQRCVKUFREFSN-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):
    3.4
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    62.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-硝基碘苯对甲基苯乙酮 在 palladium diacetate 、 三氟乙酸silver(l) oxide 作用下, 反应 20.0h, 以84%的产率得到1-(5-methyl-4'-nitrobiphenyl-2-yl)ethanone
    参考文献:
    名称:
    Synthesis of Phenanthrone Derivatives from sec-Alkyl Aryl Ketones and Aryl Halides via a Palladium-Catalyzed Dual C−H Bond Activation and Enolate Cyclization
    摘要:
    A palladium-catalyzed chelation-assisted C-H activation of alkyl aryl ketones and their reaction with aryl iodides to afford ortho-arylated products is described. For sec-alkyl aryl ketones, the catalytic reaction proceeds further to give 10,10-dialkylphenanthrone derivatives. A possible reaction mechanism involving directed dual C-H bond activation and enolate cyclization for the formation of 10,10-dialkylphenanthrone derivatives is proposed.
    DOI:
    10.1021/ja1026248
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文献信息

  • Synthesis of Phenanthrone Derivatives from <i>sec-</i>Alkyl Aryl Ketones and Aryl Halides via a Palladium-Catalyzed Dual C−H Bond Activation and Enolate Cyclization
    作者:Parthasarathy Gandeepan、Kanniyappan Parthasarathy、Chien-Hong Cheng
    DOI:10.1021/ja1026248
    日期:2010.6.30
    A palladium-catalyzed chelation-assisted C-H activation of alkyl aryl ketones and their reaction with aryl iodides to afford ortho-arylated products is described. For sec-alkyl aryl ketones, the catalytic reaction proceeds further to give 10,10-dialkylphenanthrone derivatives. A possible reaction mechanism involving directed dual C-H bond activation and enolate cyclization for the formation of 10,10-dialkylphenanthrone derivatives is proposed.
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