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7-methyl-1H-1,10-phenanthrolin-4-one | 1218756-07-0

中文名称
——
中文别名
——
英文名称
7-methyl-1H-1,10-phenanthrolin-4-one
英文别名
——
7-methyl-1H-1,10-phenanthrolin-4-one化学式
CAS
1218756-07-0
化学式
C13H10N2O
mdl
——
分子量
210.235
InChiKey
WEXVTMYSGIIOBA-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):
    2.2
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    42
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    参考文献:
    名称:
    New Nonsymmetric Phenanthrolines as Very Effective Ligands in the Palladium-Catalyzed Carbonylation of Nitrobenzene
    摘要:
    Inspired by the results of a previous mechanistic Study, a series of mostly new nonsymmetric phenanthrolines were synthesized and tested as ligands in the palladium-catalyzed reductive carbonylation reaction of nitrobenzene to methyl phenylcarbamate. Very good results were obtained when the asymmetry was of an electronic nature (a donating substituent in the para position of one of the two pyridinic rings and an electron-withdrawing or no substituent on the para position of the other pyridinic ring), but steric hindrance in the ortho or meta position retarded the reaction. The TOF for the modified system is the highest ever reported for any carbonylation reaction of nitroarenes.
    DOI:
    10.1021/om100023x
  • 作为产物:
    描述:
    参考文献:
    名称:
    New Nonsymmetric Phenanthrolines as Very Effective Ligands in the Palladium-Catalyzed Carbonylation of Nitrobenzene
    摘要:
    Inspired by the results of a previous mechanistic Study, a series of mostly new nonsymmetric phenanthrolines were synthesized and tested as ligands in the palladium-catalyzed reductive carbonylation reaction of nitrobenzene to methyl phenylcarbamate. Very good results were obtained when the asymmetry was of an electronic nature (a donating substituent in the para position of one of the two pyridinic rings and an electron-withdrawing or no substituent on the para position of the other pyridinic ring), but steric hindrance in the ortho or meta position retarded the reaction. The TOF for the modified system is the highest ever reported for any carbonylation reaction of nitroarenes.
    DOI:
    10.1021/om100023x
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文献信息

  • US7396399B2
    申请人:——
    公开号:US7396399B2
    公开(公告)日:2008-07-08
  • US7718803B2
    申请人:——
    公开号:US7718803B2
    公开(公告)日:2010-05-18
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同类化合物

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