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2-(2-Hydroxyphenyl)-3-(1,2,4-triazol-4-yl)-1,3-thiazolidin-4-one | 1141752-85-3

中文名称
——
中文别名
——
英文名称
2-(2-Hydroxyphenyl)-3-(1,2,4-triazol-4-yl)-1,3-thiazolidin-4-one
英文别名
——
2-(2-Hydroxyphenyl)-3-(1,2,4-triazol-4-yl)-1,3-thiazolidin-4-one化学式
CAS
1141752-85-3
化学式
C11H10N4O2S
mdl
——
分子量
262.292
InChiKey
WHEBHDCVNMOLCV-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

  • 熔点:
    158 °C
  • 沸点:
    453.5±55.0 °C(predicted)
  • 密度:
    1.59±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    96.6
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    (6E)-6-[(1,2,4-三唑-4-基氨基)亚甲基]环己-2,4-二烯-1-酮巯基乙酸 在 zinc(II) chloride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以58%的产率得到2-(2-Hydroxyphenyl)-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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