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2-(4-chloropyridin-2-yl)-5-methylthio-1,3,4-thiadiazole | 1192456-32-8

中文名称
——
中文别名
——
英文名称
2-(4-chloropyridin-2-yl)-5-methylthio-1,3,4-thiadiazole
英文别名
2-(4-Chloropyridin-2-yl)-5-methylsulfanyl-1,3,4-thiadiazole
2-(4-chloropyridin-2-yl)-5-methylthio-1,3,4-thiadiazole化学式
CAS
1192456-32-8
化学式
C8H6ClN3S2
mdl
——
分子量
243.741
InChiKey
QFICCCXSMWCDQL-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):
    2.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    92.2
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    二硫化碳4-chloropicolinohydrazonamide碘甲烷甲醇 为溶剂, 反应 1.0h, 以57%的产率得到2-(4-chloropyridin-2-yl)-5-methylthio-1,3,4-thiadiazole
    参考文献:
    名称:
    The Synthesis and Microbiological Activity of New 4-Chloropyridin-2-yl Derivatives
    摘要:
    4-chloropicolinamide is described. The desired compounds were formed by reactions of methyl 4-chloropicolinohydrazonamide or 4-chloro-N'-methylpicolinohydrazonamide with suitable counter partners (carbon disulfide, alkyl halides, aldehydes, ketones, carbohydrazonamides or isothiocyanates) or via 4-chloropicolinimidate, obtained by a convenient method from nitrile with catalytic amount of DBU. Selected products were screened for bacteriostatic and tuberculostatic activity. Synthesis of 4-chloropicolinamidrazone derivatives starting from
    DOI:
    10.3987/com-09-11696
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文献信息

  • The Synthesis and Microbiological Activity of New 4-Chloropyridin-2-yl Derivatives
    作者:Agnieszka Bogdanowicz、Henryk Foks、Anna Kędzia、Ewa Kwapisz、Zofia Zwolska、Ewa Augustynowicz-Kopeć
    DOI:10.3987/com-09-11696
    日期:——
    4-chloropicolinamide is described. The desired compounds were formed by reactions of methyl 4-chloropicolinohydrazonamide or 4-chloro-N'-methylpicolinohydrazonamide with suitable counter partners (carbon disulfide, alkyl halides, aldehydes, ketones, carbohydrazonamides or isothiocyanates) or via 4-chloropicolinimidate, obtained by a convenient method from nitrile with catalytic amount of DBU. Selected products were screened for bacteriostatic and tuberculostatic activity. Synthesis of 4-chloropicolinamidrazone derivatives starting from
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