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1-(5-Fluoro-2-isopropoxyphenyl)ethan-1-one | 1019529-01-1

中文名称
——
中文别名
——
英文名称
1-(5-Fluoro-2-isopropoxyphenyl)ethan-1-one
英文别名
1-(5-fluoro-2-propan-2-yloxyphenyl)ethanone
1-(5-Fluoro-2-isopropoxyphenyl)ethan-1-one化学式
CAS
1019529-01-1
化学式
C11H13FO2
mdl
MFCD11136903
分子量
196.221
InChiKey
ROOHCFGBZAITQC-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):
    2.5
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.363
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 下游产品
    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:
    1-(5-Fluoro-2-isopropoxyphenyl)ethan-1-one 在 benzyltrimethylazanium tribroman-2-uide 作用下, 生成 2-bromo-1-(5-fluoro-2-propan-2-yloxyphenyl)ethanone
    参考文献:
    名称:
    Novel hybrids from lamellarin D and combretastatin A 4 as cytotoxic agents
    摘要:
    A new series of hybrids of lamellarin D and combretastatin A 4,1,2-diphenyl-5,6-dihydropyrrolo [2,1-a] isoquinolines, were designed as cytotoxic agents based on principles of combination in medicinal chemistry and taking the parent compounds' different anti-proliferative mechanisms into consideration. Twenty-two novel hybrids were synthesized through a convenient route, with a key step of core pyrrole formation and evaluated for their anti-proliferative activities in vitro against K-562, A-549, SMMC-7721, SGC-7901 and HCF-116 cancer cell lines. The results showed that some hybrids had good anti-proliferative activities in low IC50 ranges. (C) 2009 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2009.09.017
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文献信息

  • Novel hybrids from lamellarin D and combretastatin A 4 as cytotoxic agents
    作者:Li Shen、Xiaochun Yang、Bo Yang、Qiaojun He、Yongzhou Hu
    DOI:10.1016/j.ejmech.2009.09.017
    日期:2010.1
    A new series of hybrids of lamellarin D and combretastatin A 4,1,2-diphenyl-5,6-dihydropyrrolo [2,1-a] isoquinolines, were designed as cytotoxic agents based on principles of combination in medicinal chemistry and taking the parent compounds' different anti-proliferative mechanisms into consideration. Twenty-two novel hybrids were synthesized through a convenient route, with a key step of core pyrrole formation and evaluated for their anti-proliferative activities in vitro against K-562, A-549, SMMC-7721, SGC-7901 and HCF-116 cancer cell lines. The results showed that some hybrids had good anti-proliferative activities in low IC50 ranges. (C) 2009 Elsevier Masson SAS. All rights reserved.
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