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4-(4-isopropylbenzyl)-4',4'-dimethyl-1,4-dihydro-3H-spiro[benzo[f]quinoline-2,1'-cyclohexane]2',6'-dione | 893774-25-9

中文名称
——
中文别名
——
英文名称
4-(4-isopropylbenzyl)-4',4'-dimethyl-1,4-dihydro-3H-spiro[benzo[f]quinoline-2,1'-cyclohexane]2',6'-dione
英文别名
4',4'-dimethyl-4-[4-(propan-2-yl)benzyl]-3,4-dihydro-1H,2'H,6'H-spiro[benzo[f]quinoline-2,1'-cyclohexane]-2',6'-dione;5',5'-dimethyl-4-[(4-propan-2-ylphenyl)methyl]spiro[1,3-dihydrobenzo[f]quinoline-2,2'-cyclohexane]-1',3'-dione
4-(4-isopropylbenzyl)-4',4'-dimethyl-1,4-dihydro-3H-spiro[benzo[f]quinoline-2,1'-cyclohexane]2',6'-dione化学式
CAS
893774-25-9
化学式
C30H33NO2
mdl
——
分子量
439.598
InChiKey
LULBXQJDULKYTA-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):
    6.4
  • 重原子数:
    33
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    聚合甲醛N-[(4-propan-2-ylphenyl)methyl]naphthalen-2-amine5,5-二甲基-1,3-环己二酮乙醇 为溶剂, 反应 0.17h, 以82%的产率得到4-(4-isopropylbenzyl)-4',4'-dimethyl-1,4-dihydro-3H-spiro[benzo[f]quinoline-2,1'-cyclohexane]2',6'-dione
    参考文献:
    名称:
    Condensation of N-monosubstituted 2-naphthylamines, formaldehyde, and cyclic β-diketones. One-pot synthesis of 2,4-disubstituted derivatives of 1,2,3,4-tetrahydrobenzo[f]quinoline
    摘要:
    Various spirocyclic derivatives of 1,2,3,4-tetrahydrobenzo[f]quinoline containing substituents in the positions 2 and 4 of the ring were obtained by one-pot multicomponent condensation of available N-benzyl-2-naphthylamines, formaldehyde, and cyclic beta-diketones of cyclohexanedione series.
    DOI:
    10.1134/s1070428010090113
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文献信息

  • Condensation of N-monosubstituted 2-naphthylamines, formaldehyde, and cyclic β-diketones. One-pot synthesis of 2,4-disubstituted derivatives of 1,2,3,4-tetrahydrobenzo[f]quinoline
    作者:A. P. Kadutskii、N. G. Kozlov
    DOI:10.1134/s1070428010090113
    日期:2010.9
    Various spirocyclic derivatives of 1,2,3,4-tetrahydrobenzo[f]quinoline containing substituents in the positions 2 and 4 of the ring were obtained by one-pot multicomponent condensation of available N-benzyl-2-naphthylamines, formaldehyde, and cyclic beta-diketones of cyclohexanedione series.
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