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3-(1-Methylbenzo[f]quinolin-3-yl)aniline | 609818-93-1

中文名称
——
中文别名
——
英文名称
3-(1-Methylbenzo[f]quinolin-3-yl)aniline
英文别名
——
3-(1-Methylbenzo[f]quinolin-3-yl)aniline化学式
CAS
609818-93-1
化学式
C20H16N2
mdl
——
分子量
284.36
InChiKey
BAOXNVIGIKOHJG-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):
    4.8
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    38.9
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-(1-Methylbenzo[f]quinolin-3-yl)aniline苯磺酰氯吡啶 作用下, 反应 2.0h, 以49%的产率得到N-[3-(1-methylbenzo[f]quinolin-3-yl)phenyl]benzenesulfonamide
    参考文献:
    名称:
    摘要:
    Three-component condensation of 2-aminonaphthalene, acetone, and substituted benzaldehydes in alcoholic solution in the presence of concentrated hydrochloric acid gave 3-aryl-1-methylbenzo[f]quinolines. 1-Methyl-3-(nitrophenyl)benzo[f]quinolines were reduced to the corresponding amines which were converted into amides having a sulfonyl or chloroacetyl group in the aryl substituent.
    DOI:
    10.1023/a:1026077716902
  • 作为产物:
    描述:
    1-methyl-3-(3-nitrophenyl)benzo[f]quinoline盐酸 、 tin(ll) chloride 作用下, 以 异丙醇 为溶剂, 反应 1.0h, 以52%的产率得到3-(1-Methylbenzo[f]quinolin-3-yl)aniline
    参考文献:
    名称:
    摘要:
    Three-component condensation of 2-aminonaphthalene, acetone, and substituted benzaldehydes in alcoholic solution in the presence of concentrated hydrochloric acid gave 3-aryl-1-methylbenzo[f]quinolines. 1-Methyl-3-(nitrophenyl)benzo[f]quinolines were reduced to the corresponding amines which were converted into amides having a sulfonyl or chloroacetyl group in the aryl substituent.
    DOI:
    10.1023/a:1026077716902
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文献信息

  • ——
    作者:N. G. Kozlov、L. I. Basalaeva
    DOI:10.1023/a:1026077716902
    日期:——
    Three-component condensation of 2-aminonaphthalene, acetone, and substituted benzaldehydes in alcoholic solution in the presence of concentrated hydrochloric acid gave 3-aryl-1-methylbenzo[f]quinolines. 1-Methyl-3-(nitrophenyl)benzo[f]quinolines were reduced to the corresponding amines which were converted into amides having a sulfonyl or chloroacetyl group in the aryl substituent.
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