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N1-(3-chloropropyl)-6-nitroindazole | 1016495-42-3

中文名称
——
中文别名
——
英文名称
N1-(3-chloropropyl)-6-nitroindazole
英文别名
N-(3-chloropropyl)-6-nitroindazole;1-(3-Chloropropyl)-6-nitroindazole
N1-(3-chloropropyl)-6-nitroindazole化学式
CAS
1016495-42-3
化学式
C10H10ClN3O2
mdl
——
分子量
239.661
InChiKey
OEOSWLVQRJDBEI-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

物化性质

  • 沸点:
    401.2±25.0 °C(Predicted)
  • 密度:
    1.43±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    63.6
  • 氢给体数:
    0
  • 氢受体数:
    3

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
  • 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:
    N1-(3-chloropropyl)-6-nitroindazole甲醇 为溶剂, 反应 5.5h, 生成 N-[3-(1H-6-nitroindazol-1-yl)-propyl]-N'-[(3-bromophenyl)-methylidene]-urea
    参考文献:
    名称:
    Synthesis ofN1-3-{(4-Substituted aryl-3-chloro-2-oxo-azetidine)-iminocarbamyl}-propyl-6-nitroindazole Derivatives and Their Biological Significance
    摘要:
    AbstractSynthesis ofN1‐3‐{(4‐substitute daryl‐3‐chloro‐2‐oxo‐azetidine)‐iminocarbamyl}‐propyl‐6‐nitroindazole 4a4s was conducted by a conventional method. All the compounds were synthesized and characterized by IR, 1H NMR, 13C NMR, FAB‐Mass techniques and chemical methods. All the final synthesized compounds were evaluated for their antimicrobial activity and antitubercular activity with MIC values against some selected microorganisms.
    DOI:
    10.1002/cjoc.201180311
  • 作为产物:
    描述:
    1-溴-3-氯丙烷6-硝基吲唑乙醇 为溶剂, 反应 6.3h, 以65%的产率得到N1-(3-chloropropyl)-6-nitroindazole
    参考文献:
    名称:
    SYNTHESIS OF 4-THIAZOLIDINE DERIVATIVES OF 6-NITROINDAZOLE: PHARMACEUTICAL IMPORTANCE
    摘要:
    New series of N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(substituted phenyl)-4-oxo-5-(substituted benzylidene)-1,3-thiazolidine-carboxamide, compounds 5(a-j) have been synthesized from 6-nitroindazole. Structures of all the synthesized compounds were confirmed by chemical and spectral analyses such as IR, H-1 NMR, C-13 NMR and FAB-Mass. All the synthesized compounds were screened for their antibacterial, antifungal, antitubercular and antiinflammatory activities.
    DOI:
    10.4067/s0717-97072012000100018
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文献信息

  • Synthesis ofN1-3-{(4-Substituted aryl-3-chloro-2-oxo-azetidine)-iminocarbamyl}-propyl-6-nitroindazole Derivatives and Their Biological Significance
    作者:Pushkal Samadhiya、Ritu Sharma、Santosh K. Srivastava、Savitri D. Srivastava
    DOI:10.1002/cjoc.201180311
    日期:2011.8
    AbstractSynthesis ofN1‐3‐(4‐substitute daryl‐3‐chloro‐2‐oxo‐azetidine)‐iminocarbamyl}‐propyl‐6‐nitroindazole 4a4s was conducted by a conventional method. All the compounds were synthesized and characterized by IR, 1H NMR, 13C NMR, FAB‐Mass techniques and chemical methods. All the final synthesized compounds were evaluated for their antimicrobial activity and antitubercular activity with MIC values against some selected microorganisms.
  • SYNTHESIS OF 4-THIAZOLIDINE DERIVATIVES OF 6-NITROINDAZOLE: PHARMACEUTICAL IMPORTANCE
    作者:PUSHKAL SAMADHIYA、RITU SHARMA、SANTOSH K SRIVASTAV、SAVITRI D SRIVASTAVA
    DOI:10.4067/s0717-97072012000100018
    日期:——
    New series of N-[3-(1H-6-nitroindazol-1-yl)-propyl]-2-(substituted phenyl)-4-oxo-5-(substituted benzylidene)-1,3-thiazolidine-carboxamide, compounds 5(a-j) have been synthesized from 6-nitroindazole. Structures of all the synthesized compounds were confirmed by chemical and spectral analyses such as IR, H-1 NMR, C-13 NMR and FAB-Mass. All the synthesized compounds were screened for their antibacterial, antifungal, antitubercular and antiinflammatory activities.
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