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[4-(2-Hydroxy-ethyl)-5-pyrazin-2-yl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide

中文名称
——
中文别名
——
英文名称
[4-(2-Hydroxy-ethyl)-5-pyrazin-2-yl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide
英文别名
2-[[4-(2-Hydroxyethyl)-5-pyrazin-2-yl-1,2,4-triazol-3-yl]sulfanyl]acetohydrazide;2-[[4-(2-hydroxyethyl)-5-pyrazin-2-yl-1,2,4-triazol-3-yl]sulfanyl]acetohydrazide
[4-(2-Hydroxy-ethyl)-5-pyrazin-2-yl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide化学式
CAS
——
化学式
C10H13N7O2S
mdl
——
分子量
295.325
InChiKey
WLPSOXLOCISYBV-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):
    -2.3
  • 重原子数:
    20
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    157
  • 氢给体数:
    3
  • 氢受体数:
    8

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

反应信息

  • 作为产物:
    描述:
    N'-(pyrazine-2-carbonyl)-hydrazinecarbodithioic acid methyl ester 在 氢氧化钾一水合肼 作用下, 以 1,4-二氧六环乙醇 为溶剂, 反应 2.0h, 生成 [4-(2-Hydroxy-ethyl)-5-pyrazin-2-yl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide
    参考文献:
    名称:
    STUDIES ON PYRAZINE DERIVATIVES. XL. SYNTHESIS, REACTIVITY, AND TUBERCULOSTATIC ACTIVITY OF 4-HYDROXYALKYL-5-PYRAZINYL4H-[1,2,4]-TRIAZOLE-3-THIONES
    摘要:
    In the reactions of pirazinoyldithiocarbazoic acid monoester with aminoalcohols, 4-hydroxyalkyl-1,2,4-triazole-3-thiones were obtained. Their susceptibility to alkylation, as well as the condensed heterocyclic 1,3-thiazacycloalkyl[3,2-b]-1,2,4-thiazoles(1) formation ability, were examined. Some of the compounds obtained were tested for their tuberculostatic activity.
    DOI:
    10.1080/10426500490485534
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文献信息

  • STUDIES ON PYRAZINE DERIVATIVES. XL. SYNTHESIS, REACTIVITY, AND TUBERCULOSTATIC ACTIVITY OF 4-HYDROXYALKYL-5-PYRAZINYL4H-[1,2,4]-TRIAZOLE-3-THIONES
    作者:Henryk Foks、Mieczysław Janowiec、Zofia Zwolska、Ewa Augustynowicz-Kopeć
    DOI:10.1080/10426500490485534
    日期:2004.12.1
    In the reactions of pirazinoyldithiocarbazoic acid monoester with aminoalcohols, 4-hydroxyalkyl-1,2,4-triazole-3-thiones were obtained. Their susceptibility to alkylation, as well as the condensed heterocyclic 1,3-thiazacycloalkyl[3,2-b]-1,2,4-thiazoles(1) formation ability, were examined. Some of the compounds obtained were tested for their tuberculostatic activity.
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