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dimethyl 3-(4-nitrophenyl)-3,4-dihydrobenzo[f]quinoline-1,2-dicarboxylate | 1433876-61-9

中文名称
——
中文别名
——
英文名称
dimethyl 3-(4-nitrophenyl)-3,4-dihydrobenzo[f]quinoline-1,2-dicarboxylate
英文别名
Dimethyl 3-(4-nitrophenyl)-3,4-dihydrobenzo[f]quinoline-1,2-dicarboxylate
dimethyl 3-(4-nitrophenyl)-3,4-dihydrobenzo[f]quinoline-1,2-dicarboxylate化学式
CAS
1433876-61-9
化学式
C23H18N2O6
mdl
——
分子量
418.406
InChiKey
PPGHLIPZYRKDMF-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):
    4.2
  • 重原子数:
    31
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    110
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    对硝基苯甲醛2-萘胺丁炔二酸二甲酯三氯化锑 作用下, 以 乙腈 为溶剂, 反应 6.0h, 以77%的产率得到dimethyl 3-(4-nitrophenyl)-3,4-dihydrobenzo[f]quinoline-1,2-dicarboxylate
    参考文献:
    名称:
    One pot imino Diels–Alder reaction for the synthesis of 3-aryl-3,4-dihydrobenzo[f]quinoline derivatives catalyzed by antimony trichloride
    摘要:
    An one pot simple and efficient approach toward the synthesis of dialkyl-3-aryl-3,4-dihydrobenzo[f]quinoline-1,2-dicarboxylate and its dehydro derivatives have been developed through the three-component reaction of aromatic aldehydes, 2-naphthylamine, and but-2-ynedioate catalyzed by SbCl3 under reflux in acetonitrile in good to excellent yields. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.03.093
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文献信息

  • One pot imino Diels–Alder reaction for the synthesis of 3-aryl-3,4-dihydrobenzo[f]quinoline derivatives catalyzed by antimony trichloride
    作者:Gourhari Maiti、Rajiv Karmakar、Utpal Kayal
    DOI:10.1016/j.tetlet.2013.03.093
    日期:2013.6
    An one pot simple and efficient approach toward the synthesis of dialkyl-3-aryl-3,4-dihydrobenzo[f]quinoline-1,2-dicarboxylate and its dehydro derivatives have been developed through the three-component reaction of aromatic aldehydes, 2-naphthylamine, and but-2-ynedioate catalyzed by SbCl3 under reflux in acetonitrile in good to excellent yields. (C) 2013 Elsevier Ltd. All rights reserved.
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