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picolinic acid N1-(2-benzothienylmethylene)amidrazone

中文名称
——
中文别名
——
英文名称
picolinic acid N1-(2-benzothienylmethylene)amidrazone
英文别名
N'-(1-benzothiophen-2-ylmethylideneamino)pyridine-2-carboximidamide
picolinic acid N<sup>1</sup>-(2-benzothienylmethylene)amidrazone化学式
CAS
——
化学式
C15H12N4S
mdl
——
分子量
280.353
InChiKey
ZDZHJPSEOZTQMM-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):
    3.04
  • 重原子数:
    20.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    63.63
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    1-苯并噻酚-2-羧醛2-吡啶氨基腙乙醇 为溶剂, 以83%的产率得到picolinic acid N1-(2-benzothienylmethylene)amidrazone
    参考文献:
    名称:
    NewN1-Hetarylmethylene-Substituted Amidrazones with Potential Antimycobacterial Activity
    摘要:
    N-1-Hetarylmethylene (e.g. pyridyl, 2-benzoxazolyl, 2-benzofuryl) substituted picolinic acid amidrazones and pyrazine-2-carboxamidrazones were investigated. The compounds were accessible by reaction of the unsubstituted amidrazones with aldehydes. Pyrazine-2-carbox-N-1-(2-benzoxazolymethylene)amidrazones were obtained by a new multistep reaction. The investigated amidrazones were tested for their antibacterial activity against four strains of mycobacteria (M. tuberculosis, M. avium, M. intracellulare, M. lufu) and were shown to have rather low activity.
    DOI:
    10.1002/(sici)1521-4184(199912)332:12<427::aid-ardp427>3.0.co;2-h
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文献信息

  • NewN1-Hetarylmethylene-Substituted Amidrazones with Potential Antimycobacterial Activity
    作者:Donald Ranft、Torsten Seyfarth、Klaus-Jürgen Schaper、Gudrun Lehwark-Yvetot、Clemens Bruhn、Axel Büge
    DOI:10.1002/(sici)1521-4184(199912)332:12<427::aid-ardp427>3.0.co;2-h
    日期:1999.12
    N-1-Hetarylmethylene (e.g. pyridyl, 2-benzoxazolyl, 2-benzofuryl) substituted picolinic acid amidrazones and pyrazine-2-carboxamidrazones were investigated. The compounds were accessible by reaction of the unsubstituted amidrazones with aldehydes. Pyrazine-2-carbox-N-1-(2-benzoxazolymethylene)amidrazones were obtained by a new multistep reaction. The investigated amidrazones were tested for their antibacterial activity against four strains of mycobacteria (M. tuberculosis, M. avium, M. intracellulare, M. lufu) and were shown to have rather low activity.
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