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2-[(3-methylphenyl)thio]pyrimidine | 646511-17-3

中文名称
——
中文别名
——
英文名称
2-[(3-methylphenyl)thio]pyrimidine
英文别名
Pyrimidine, 2-[(3-methylphenyl)thio]-;2-(3-methylphenyl)sulfanylpyrimidine
2-[(3-methylphenyl)thio]pyrimidine化学式
CAS
646511-17-3
化学式
C11H10N2S
mdl
MFCD27926904
分子量
202.28
InChiKey
JLUPCQAWUBGZCN-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

  • 沸点:
    378.3±35.0 °C(Predicted)
  • 密度:
    1.21±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    51.1
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:0f2afd48d26901ad041a4c5350cfd716
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反应信息

  • 作为产物:
    描述:
    2-氯嘧啶3-甲基苯硫酚potassium tert-butylate 作用下, 以 异丙醇 为溶剂, 以66%的产率得到2-[(3-methylphenyl)thio]pyrimidine
    参考文献:
    名称:
    Antimycobacterial Agents. 1. Thio Analogues of Purine
    摘要:
    Thio analogues of purine, pyridine, and pyrimidine were prepared based on the initial activity screening of several analogues of these heterocycles against Mycobacterium tuberculosis (Mtb). Certain 6-thio-substituted purine analogues described herein showed moderate to good inhibitory activity. In particular, two purine analogues 9-(ethylcarboxymethyl)-6-(decylthio)9H-purine (20) and 9-(ethylcarboxymethyl)-6-(dodecylthio)-9H-purine (21) exhibited MIC values of 1.56 and 0.78 mug/mL respectively against the Mtb H(37)Rv strain. N-9-Substitution apparently enhances the antimycobacterial activity in the purine series described herein.
    DOI:
    10.1021/jm030389b
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文献信息

  • Antimycobacterial Agents. 1. Thio Analogues of Purine
    作者:Ashish K. Pathak、Vibha Pathak、Lainne E. Seitz、William J. Suling、Robert C. Reynolds
    DOI:10.1021/jm030389b
    日期:2004.1.1
    Thio analogues of purine, pyridine, and pyrimidine were prepared based on the initial activity screening of several analogues of these heterocycles against Mycobacterium tuberculosis (Mtb). Certain 6-thio-substituted purine analogues described herein showed moderate to good inhibitory activity. In particular, two purine analogues 9-(ethylcarboxymethyl)-6-(decylthio)9H-purine (20) and 9-(ethylcarboxymethyl)-6-(dodecylthio)-9H-purine (21) exhibited MIC values of 1.56 and 0.78 mug/mL respectively against the Mtb H(37)Rv strain. N-9-Substitution apparently enhances the antimycobacterial activity in the purine series described herein.
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