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5-(4-Chloro-phenyl)-2-(2-hydroxy-ethyl)-1,2-dihydro-[1,2,4]triazole-3-thione | 223794-11-4

中文名称
——
中文别名
——
英文名称
5-(4-Chloro-phenyl)-2-(2-hydroxy-ethyl)-1,2-dihydro-[1,2,4]triazole-3-thione
英文别名
——
5-(4-Chloro-phenyl)-2-(2-hydroxy-ethyl)-1,2-dihydro-[1,2,4]triazole-3-thione化学式
CAS
223794-11-4
化学式
C10H10ClN3OS
mdl
——
分子量
255.728
InChiKey
NIJJQEIDKSQFAW-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):
    2.25
  • 重原子数:
    16.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    53.84
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    环丙基甲酰氯5-(4-Chloro-phenyl)-2-(2-hydroxy-ethyl)-1,2-dihydro-[1,2,4]triazole-3-thione吡啶 作用下, 以 甲苯 为溶剂, 以80%的产率得到2-[5-(4-chlorophenyl)-3-sulfanylidene-1H-1,2,4-triazol-2-yl]ethyl cyclopropanecarboxylate
    参考文献:
    名称:
    Synthesis and anti-inflammatory activity of esters derived from 5-aryl-1,2-dihydro-2-(2-hydroxyethyl)-3H-1,2,4-triazole-3-thiones
    摘要:
    Some aliphatic and aromatic esters 2a-l were prepared starting from 5-aryl-1,2,4-triazoline-3-thiones bearing a 2-hydroxyethyl chain in position 2. The title compounds were evaluated for antipyretic and anti-inflammatory activities. Nearly all derivatives and in particular 2f, 2h, 2k exhibited antiphlogistic properties but were lacking in antipyretic activity. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(98)00074-3
  • 作为产物:
    描述:
    2-肼基乙醇异硫氰酸 p-氯苯甲酰脂对甲苯磺酸 作用下, 以 为溶剂, 反应 3.0h, 以70%的产率得到5-(4-Chloro-phenyl)-2-(2-hydroxy-ethyl)-1,2-dihydro-[1,2,4]triazole-3-thione
    参考文献:
    名称:
    Synthesis and anti-inflammatory activity of esters derived from 5-aryl-1,2-dihydro-2-(2-hydroxyethyl)-3H-1,2,4-triazole-3-thiones
    摘要:
    Some aliphatic and aromatic esters 2a-l were prepared starting from 5-aryl-1,2,4-triazoline-3-thiones bearing a 2-hydroxyethyl chain in position 2. The title compounds were evaluated for antipyretic and anti-inflammatory activities. Nearly all derivatives and in particular 2f, 2h, 2k exhibited antiphlogistic properties but were lacking in antipyretic activity. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(98)00074-3
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