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6,7-Dimethoxy-2-(3-phenyl-propyl)-3,4-dihydro-2H-isoquinolin-1-one | 803705-91-1

中文名称
——
中文别名
——
英文名称
6,7-Dimethoxy-2-(3-phenyl-propyl)-3,4-dihydro-2H-isoquinolin-1-one
英文别名
6,7-Dimethoxy-2-(3-phenylpropyl)-3,4-dihydroisoquinolin-1(2H)-one;6,7-dimethoxy-2-(3-phenylpropyl)-3,4-dihydroisoquinolin-1-one
6,7-Dimethoxy-2-(3-phenyl-propyl)-3,4-dihydro-2H-isoquinolin-1-one化学式
CAS
803705-91-1
化学式
C20H23NO3
mdl
——
分子量
325.408
InChiKey
GFLBLQDPOYGUKX-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):
    3.7
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3,4-二甲氧基苯乙胺对硝基苯基氯甲酸酯 、 alkaline earth salt of/the/ methylsulfuric acid 以61%的产率得到6,7-Dimethoxy-2-(3-phenyl-propyl)-3,4-dihydro-2H-isoquinolin-1-one
    参考文献:
    名称:
    Solid-phase synthesis of isoquinolinones using Bischler–Napieralski cyclization
    摘要:
    Isoquinolinone is a structural unit found in many natural products having various important biological activities. A traceless solid-phase synthetic approach has been developed to prepare isoquinolinone derivatives. This approach enables one to synthesize isoquinolinones having various moieties on benzene nuclei and also can produce derivatives with a proton on the amide nitrogen. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.09.059
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文献信息

  • Solid-phase synthesis of isoquinolinones using Bischler–Napieralski cyclization
    作者:Meei-Shiou Chern、Wen-Ren Li
    DOI:10.1016/j.tetlet.2004.09.059
    日期:2004.11
    Isoquinolinone is a structural unit found in many natural products having various important biological activities. A traceless solid-phase synthetic approach has been developed to prepare isoquinolinone derivatives. This approach enables one to synthesize isoquinolinones having various moieties on benzene nuclei and also can produce derivatives with a proton on the amide nitrogen. (C) 2004 Elsevier Ltd. All rights reserved.
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