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N-(2-phenylethyl)piperidine-1-carbothioamide | 502740-53-6

中文名称
——
中文别名
——
英文名称
N-(2-phenylethyl)piperidine-1-carbothioamide
英文别名
N-phenethylpiperidine-1-carbothioamide
N-(2-phenylethyl)piperidine-1-carbothioamide化学式
CAS
502740-53-6
化学式
C14H20N2S
mdl
MFCD02754242
分子量
248.392
InChiKey
MGICFDHZUDIPGA-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):
    3
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    47.4
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    哌啶二硫化碳2-苯乙胺 在 sodium hydroxide 作用下, 以 为溶剂, 反应 10.0h, 以82%的产率得到N-(2-phenylethyl)piperidine-1-carbothioamide
    参考文献:
    名称:
    A Concise Synthesis of Substituted Thiourea Derivatives in Aqueous Medium
    摘要:
    An efficient method for the synthesis of symmetrical and unsymmetrical substituted thiourea derivatives by means of simple condensation between available building blocks such Lis airlines and carbon disulfide in aqueous medium is presented. This protocol works smoothly with aliphatic primary amines to afford various di- and trisubstituted thiourea derivatives. The present method is also useful ill synthesizing various substituted 2-mercapto imidazole heterocycles. This method proceeds through a xanthate (amino dithiol deivative) intermediate, unlike isothiocyanate as in all earlier known method.
    DOI:
    10.1021/jo1001593
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文献信息

  • A Concise Synthesis of Substituted Thiourea Derivatives in Aqueous Medium
    作者:Mahagundappa R. Maddani、Kandikere R. Prabhu
    DOI:10.1021/jo1001593
    日期:2010.4.2
    An efficient method for the synthesis of symmetrical and unsymmetrical substituted thiourea derivatives by means of simple condensation between available building blocks such Lis airlines and carbon disulfide in aqueous medium is presented. This protocol works smoothly with aliphatic primary amines to afford various di- and trisubstituted thiourea derivatives. The present method is also useful ill synthesizing various substituted 2-mercapto imidazole heterocycles. This method proceeds through a xanthate (amino dithiol deivative) intermediate, unlike isothiocyanate as in all earlier known method.
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