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dimethylamino-trifluoromethyl-sulfoxide | 30957-46-1

中文名称
——
中文别名
——
英文名称
dimethylamino-trifluoromethyl-sulfoxide
英文别名
Trifluormethylsulfinsaeurediethylamid;N,N-Diethyl-trifluormethylsulfinamid;Methanesulfen-amide, N,N-diethyl-1,1,1-trifluoro;N,N-diethyl-1,1,1-trifluoromethanesulfinamide
dimethylamino-trifluoromethyl-sulfoxide化学式
CAS
30957-46-1
化学式
C5H10F3NOS
mdl
——
分子量
189.202
InChiKey
FIUDFKCMXNJQLV-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:
    158.9±50.0 °C(Predicted)
  • 密度:
    1.311±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    39.5
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis of Trifluoromethanesulfinamidines and -sulfanylamides
    摘要:
    Fluorinated moieties constitute important substituents used in many applications to modify the properties of molecules. The action of DAST onto Ruppert's rea gent yields to a not isolable intermediate that can then react with various primary amines to give trifluoromethanesulfinamidines and trifluoromethanesulfanylamides. Such compounds were unknown until now and constitute interesting new families of fluorinated molecules.
    DOI:
    10.1021/jo8018544
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文献信息

  • Sauer, Dennis T.; Shreeve, Jean'ne M., Inorganic Chemistry, 1971, vol. 10, # 2, p. 358 - 362
    作者:Sauer, Dennis T.、Shreeve, Jean'ne M.
    DOI:——
    日期:——
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: F: PerFHalOrg.2, 1.2, page 50 - 76
    作者:
    DOI:——
    日期:——
  • Synthesis of Trifluoromethanesulfinamidines and -sulfanylamides
    作者:Aurélien Ferry、Thierry Billard、Bernard R. Langlois、Eric Bacqué
    DOI:10.1021/jo8018544
    日期:2008.12.5
    Fluorinated moieties constitute important substituents used in many applications to modify the properties of molecules. The action of DAST onto Ruppert's rea gent yields to a not isolable intermediate that can then react with various primary amines to give trifluoromethanesulfinamidines and trifluoromethanesulfanylamides. Such compounds were unknown until now and constitute interesting new families of fluorinated molecules.
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