摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-(3-Mercapto-5-pyrazin-2-yl-[1,2,4]triazol-4-yl)-propan-2-ol | 717847-08-0

中文名称
——
中文别名
——
英文名称
1-(3-Mercapto-5-pyrazin-2-yl-[1,2,4]triazol-4-yl)-propan-2-ol
英文别名
4-(2-hydroxypropyl)-3-pyrazin-2-yl-1H-1,2,4-triazole-5-thione
1-(3-Mercapto-5-pyrazin-2-yl-[1,2,4]triazol-4-yl)-propan-2-ol化学式
CAS
717847-08-0
化学式
C9H11N5OS
mdl
——
分子量
237.285
InChiKey
GAKXKQLKZBGOMJ-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):
    -0.4
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    106
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    1-(3-Mercapto-5-pyrazin-2-yl-[1,2,4]triazol-4-yl)-propan-2-ol 在 PPA 作用下, 以50%的产率得到6-Methyl-3-pyrazin-2-yl-5,6-dihydro-thiazolo[2,3-c][1,2,4]triazole
    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
  • 作为产物:
    描述:
    异丙醇胺N'-(pyrazine-2-carbonyl)-hydrazinecarbodithioic acid methyl ester 反应 0.5h, 以81%的产率得到1-(3-Mercapto-5-pyrazin-2-yl-[1,2,4]triazol-4-yl)-propan-2-ol
    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
点击查看最新优质反应信息