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2-(5-nitroindazol-1-yl)acetohydrazide | 1245567-13-8

中文名称
——
中文别名
——
英文名称
2-(5-nitroindazol-1-yl)acetohydrazide
英文别名
5-nitroindazole-1-ylacethydrazide
2-(5-nitroindazol-1-yl)acetohydrazide化学式
CAS
1245567-13-8
化学式
C9H9N5O3
mdl
——
分子量
235.202
InChiKey
DGAWJHVAENNJEY-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):
    0.1
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    119
  • 氢给体数:
    2
  • 氢受体数:
    5

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:
    2-(5-nitroindazol-1-yl)acetohydrazide 在 sodium hydroxide 作用下, 以 甲醇 为溶剂, 反应 4.0h, 生成 3-[(5-nitroindazol-1-yl)methyl]-4-phenyl-1H-1,2,4-triazole-5-thione
    参考文献:
    名称:
    Synthesis and Antimicrobial Activity of New Derivatives of 1,3,4-Thiadiazoles and 1,2,4-Triazoles with 5-Nitroindazole as Support
    摘要:
    The synthesis of new derivatives of 1,3,4‐thiadiazoles and 1,2,4‐triazoles was achieved using the 1,4‐disubstituted thiosemicarbazides as intermediaries.
    DOI:
    10.1002/jhet.1738
  • 作为产物:
    描述:
    N-(ethyl ethanoate)-5-nitroindazole 在 一水合肼 作用下, 以 1,4-二氧六环 为溶剂, 反应 8.0h, 以80%的产率得到2-(5-nitroindazol-1-yl)acetohydrazide
    参考文献:
    名称:
    Synthesis and Characterization of New 2-Oxo-azetidine Derivatives
    摘要:
    Several new N-[(4-aryl-3-chloro-2-oxo-azetidine)acetamidyl]-5-nitroindazoles 4a-l were synthesized from N-(arylidene amino acetamidyl)-5-nitroindazoles 3a-l. The structures of all these compounds were confirmed by infrared, H-1 NMR, C-13 NMR, and fast atom bombardment-mass spectra and also by microanalytical data.
    DOI:
    10.1080/00397911.2010.515328
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文献信息

  • Upadhyay, Apoorva; Srivastava; Srivastava, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2011, vol. 50, # 1, p. 89 - 97
    作者:Upadhyay, Apoorva、Srivastava、Srivastava、Yadav
    DOI:——
    日期:——
  • Conventional and microwave assisted synthesis of Some new N-[(4-oxo-2-substituted aryl −1, 3-thiazolidine)-acetamidyl]-5-nitroindazoles and its antimicrobial activity
    作者:Apoorva Upadhyay、S.K. Srivastava、S.D. Srivastava
    DOI:10.1016/j.ejmech.2010.04.029
    日期:2010.9
    Several new N-[(4-oxo-2-substituted aryl-1, 3-thiazolidine)-acetamidyl]-5-nitroindazoles (4a-1) were synthesized from N-(arylidene amino acetamidyl)-5-nitroindazoles (3a-1). The reactions were carried out by both conventional as well as microwave method. The structures of these compounds were confirmed by IR, H-1 NMR, C-13 NMR, FAB-mass spectra and also by microanalytical data. The newly synthesized compounds were evaluated for their antimicrobial activity against variety of bacterial and fungal strains. The compounds 4g and 4h showed the maximum antibacterial activity (MIC 11 and 10 mu g/mL) against Escherichia coli and antifungal activity (MIC 9 and 8 mu g/mL) against Fusarium oxysporum. (C) 2010 Elsevier Masson SAS. All rights reserved.
  • Synthesis and Characterization of New 2-Oxo-azetidine Derivatives
    作者:Apoorva Upadhyay、S. K. Srivastava、S. D. Srivastava
    DOI:10.1080/00397911.2010.515328
    日期:2011.9.1
    Several new N-[(4-aryl-3-chloro-2-oxo-azetidine)acetamidyl]-5-nitroindazoles 4a-l were synthesized from N-(arylidene amino acetamidyl)-5-nitroindazoles 3a-l. The structures of all these compounds were confirmed by infrared, H-1 NMR, C-13 NMR, and fast atom bombardment-mass spectra and also by microanalytical data.
  • Synthesis and Antimicrobial Activity of New Derivatives of 1,3,4-Thiadiazoles and 1,2,4-Triazoles with 5-Nitroindazole as Support
    作者:Corina Cheptea、Valeriu Sunel、Jacques Desbrieres、Marcel Popa
    DOI:10.1002/jhet.1738
    日期:2013.3
    The synthesis of new derivatives of 1,3,4‐thiadiazoles and 1,2,4‐triazoles was achieved using the 1,4‐disubstituted thiosemicarbazides as intermediaries.
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