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2-(4-Methoxyphenyl)-3-(1,2,4-triazol-4-yl)-1,3-thiazolidin-4-one | 1025447-91-9

中文名称
——
中文别名
——
英文名称
2-(4-Methoxyphenyl)-3-(1,2,4-triazol-4-yl)-1,3-thiazolidin-4-one
英文别名
——
2-(4-Methoxyphenyl)-3-(1,2,4-triazol-4-yl)-1,3-thiazolidin-4-one化学式
CAS
1025447-91-9
化学式
C12H12N4O2S
mdl
——
分子量
276.319
InChiKey
VZYCWXHIAMMKRV-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):
    1.3
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    85.6
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    巯基乙酸1-(4-甲氧基苯基)-N-(1,2,4-三唑-4-基)甲亚胺 在 zinc(II) chloride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以68%的产率得到2-(4-Methoxyphenyl)-3-(1,2,4-triazol-4-yl)-1,3-thiazolidin-4-one
    参考文献:
    名称:
    Synthesis and Biological Activity of 3-[4H-(1,2,4)-triazolyl]-2-aryl-1,3-thiazolidin-4-ones
    摘要:
    4-Amino-1,2,4-triazole (1) undergoes facile condensation with aromatic aldehydes to afford the corresponding 4-(arylidene-amino)-4H-[1,2,4]-triazole (2 a-h) in good yields. Cyclocondensation of compounds (2 a-h) with thioglycolic acid yields 3-[4H-(1,2,4)-triazolyl]-2-aryl-1,3-thiazolidin-4-ones (3 a-h). The structures of these compounds were established on the basis of analytical and spectral data. The newly synthesized compounds were evaluated for their antibacterial and antifungal activities.
    DOI:
    10.1080/10426500801963772
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文献信息

  • Synthesis and Biological Activity of 3-[4<i>H</i>-(1,2,4)-triazolyl]-2-aryl-1,3-thiazolidin-4-ones
    作者:H. S. Patel、K. B. Patel
    DOI:10.1080/10426500801963772
    日期:2008.9.15
    4-Amino-1,2,4-triazole (1) undergoes facile condensation with aromatic aldehydes to afford the corresponding 4-(arylidene-amino)-4H-[1,2,4]-triazole (2 a-h) in good yields. Cyclocondensation of compounds (2 a-h) with thioglycolic acid yields 3-[4H-(1,2,4)-triazolyl]-2-aryl-1,3-thiazolidin-4-ones (3 a-h). The structures of these compounds were established on the basis of analytical and spectral data. The newly synthesized compounds were evaluated for their antibacterial and antifungal activities.
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