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6-fluoro-2-oxo-1,2-dihydroquinoline-4-carbohydrazide | 1388844-25-4

中文名称
——
中文别名
——
英文名称
6-fluoro-2-oxo-1,2-dihydroquinoline-4-carbohydrazide
英文别名
6-fluoro-2-oxo-1H-quinoline-4-carbohydrazide
6-fluoro-2-oxo-1,2-dihydroquinoline-4-carbohydrazide化学式
CAS
1388844-25-4
化学式
C10H8FN3O2
mdl
——
分子量
221.191
InChiKey
MSVJRDLQRHACNJ-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):
    -0.3
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    84.2
  • 氢给体数:
    3
  • 氢受体数:
    4

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

  • 作为产物:
    描述:
    ethyl 6-fluoro-2-oxo-1,2-dihydroquinoline-4-carboxylate一水合肼 作用下, 以 乙醇 为溶剂, 以70%的产率得到6-fluoro-2-oxo-1,2-dihydroquinoline-4-carbohydrazide
    参考文献:
    名称:
    Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents
    摘要:
    A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.05.096
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文献信息

  • Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents
    作者:Balakrishna Dulla、Baojie Wan、Scott G. Franzblau、Ravikumar Kapavarapu、Oliver Reiser、Javed Iqbal、Manojit Pal
    DOI:10.1016/j.bmcl.2012.05.096
    日期:2012.7
    A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent. (C) 2012 Elsevier Ltd. All rights reserved.
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