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13-[4-(2-fluorobenzyloxy)phenyl]-7,13-dihydro-12H-benzo[f]indeno[1,2-b]quinolin-12-one | 447456-63-5

中文名称
——
中文别名
——
英文名称
13-[4-(2-fluorobenzyloxy)phenyl]-7,13-dihydro-12H-benzo[f]indeno[1,2-b]quinolin-12-one
英文别名
13-{4-[(2-fluorobenzyl)oxy]phenyl}-7,13-dihydro-12H-benzo[f]indeno[1,2-b]quinolin-12-one;12-[4-[(2-fluorophenyl)methoxy]phenyl]-2-azapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(13),3(11),4,6,8,14,16,18,20-nonaen-10-one
13-[4-(2-fluorobenzyloxy)phenyl]-7,13-dihydro-12H-benzo[f]indeno[1,2-b]quinolin-12-one化学式
CAS
447456-63-5
化学式
C33H22FNO2
mdl
——
分子量
483.542
InChiKey
QGUYZJWCMUQQLW-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):
    7.5
  • 重原子数:
    37
  • 可旋转键数:
    4
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    13-[4-(2-fluorobenzyloxy)phenyl]-7,13-dihydro-12H-benzo[f]indeno[1,2-b]quinolin-12-one硝基苯 为溶剂, 反应 8.0h, 以79%的产率得到13-[4-(2-fluorobenzyloxy)phenyl]-12H-benzo[f]indeno[1,2-b]quinolin-12-one
    参考文献:
    名称:
    Condensation of fluorosubstituted benzaldehydes with amines and cyclic 1,3-diketones
    摘要:
    Condensation of fluorosubstituted benzaldehydes with 2-naphthyl or 6-quinolylamine and cyclic beta-diketones (,3-cyclohexanedione, dimedone, and 1,3-indandione) provided new fluoroderivatives of benzo[a]acridine, 4,7-phenanthroline, and benzo[f]indeno[1,2-b]quinoline. Forming in the course of the reaction fluorophenylmethylene-2-naphthyl-(or 6-quinolyl)amines, arylbis(cyclohexane-1,3-dion-2-yl)methanes, and 2-(fluorophenylmethylene)- 1,3-indandiones were isolated.
    DOI:
    10.1134/s107042800611011x
  • 作为产物:
    参考文献:
    名称:
    Condensation of fluorosubstituted benzaldehydes with amines and cyclic 1,3-diketones
    摘要:
    Condensation of fluorosubstituted benzaldehydes with 2-naphthyl or 6-quinolylamine and cyclic beta-diketones (,3-cyclohexanedione, dimedone, and 1,3-indandione) provided new fluoroderivatives of benzo[a]acridine, 4,7-phenanthroline, and benzo[f]indeno[1,2-b]quinoline. Forming in the course of the reaction fluorophenylmethylene-2-naphthyl-(or 6-quinolyl)amines, arylbis(cyclohexane-1,3-dion-2-yl)methanes, and 2-(fluorophenylmethylene)- 1,3-indandiones were isolated.
    DOI:
    10.1134/s107042800611011x
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文献信息

  • Condensation of fluorosubstituted benzaldehydes with amines and cyclic 1,3-diketones
    作者:N. G. Kozlov、K. N. Gusak
    DOI:10.1134/s107042800611011x
    日期:2006.11
    Condensation of fluorosubstituted benzaldehydes with 2-naphthyl or 6-quinolylamine and cyclic beta-diketones (,3-cyclohexanedione, dimedone, and 1,3-indandione) provided new fluoroderivatives of benzo[a]acridine, 4,7-phenanthroline, and benzo[f]indeno[1,2-b]quinoline. Forming in the course of the reaction fluorophenylmethylene-2-naphthyl-(or 6-quinolyl)amines, arylbis(cyclohexane-1,3-dion-2-yl)methanes, and 2-(fluorophenylmethylene)- 1,3-indandiones were isolated.
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