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2-dipropoxyphosphinothioylsulfanylacetic acid | 31224-81-4

中文名称
——
中文别名
——
英文名称
2-dipropoxyphosphinothioylsulfanylacetic acid
英文别名
——
2-dipropoxyphosphinothioylsulfanylacetic acid化学式
CAS
31224-81-4
化学式
C8H17O4PS2
mdl
——
分子量
272.326
InChiKey
UWWOIXUOJDPLCV-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:
    359.6±44.0 °C(Predicted)
  • 密度:
    1.272±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.88
  • 重原子数:
    15.0
  • 可旋转键数:
    9.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    55.76
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    2-dipropoxyphosphinothioylsulfanylacetic acid3,3-dimethyl-1-(1,2,4-triazol-1-yl)-1-bromo-2-butanone三乙胺 作用下, 以 丙酮 为溶剂, 以65.6%的产率得到[3,3-Dimethyl-2-oxo-1-(1,2,4-triazol-1-yl)butyl] 2-dipropoxyphosphinothioylsulfanylacetate
    参考文献:
    名称:
    Synthesis and Biological Activities of O, O-Dialkyl-dithiophosphoryl-S-acetoxy Triazolo Compounds
    摘要:
    In this article, we introduce organic phosphorus moiety into triazole ring to prepare O-dialkyl-dithiophosphoryl-S-acetoxy triazolo compounds and characterize their structures by elementary analysis and (HNMR)-H-1 and IR spectral data. From the results of biological activity screening, we found that the O-dialkyl-dithiophosphoryl-S-acetoxy triazolo compounds show lower fungicidal activities and their structures need to be optimized for the better.
    DOI:
    10.1080/10426500307939
  • 作为产物:
    描述:
    potassium O,O'-dipropyl dithiophosphate氯乙酸丙酮 为溶剂, 以86.9%的产率得到2-dipropoxyphosphinothioylsulfanylacetic acid
    参考文献:
    名称:
    Synthesis and Biological Activities of O, O-Dialkyl-dithiophosphoryl-S-acetoxy Triazolo Compounds
    摘要:
    In this article, we introduce organic phosphorus moiety into triazole ring to prepare O-dialkyl-dithiophosphoryl-S-acetoxy triazolo compounds and characterize their structures by elementary analysis and (HNMR)-H-1 and IR spectral data. From the results of biological activity screening, we found that the O-dialkyl-dithiophosphoryl-S-acetoxy triazolo compounds show lower fungicidal activities and their structures need to be optimized for the better.
    DOI:
    10.1080/10426500307939
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文献信息

  • Substitution Reactions of Mono- and Trichloro Acetic Acids with Ammonium Dialkyl (Alkylene) Dithiophosphates
    作者:Neelam Harkut、Padam N. Nagar
    DOI:10.1080/10426500600892693
    日期:2007.1.1
    A reaction of mono- and trichloro acetic acid with ammonium salts of alkylene ( dialkyl) dithiophosphate; [ OGOPS(2)NH(4); G=-CH2CH2CHMe-, -C( Me)(2)C( Me)(2)-, -CH2C( Me)(2)CH2-, and -C( Me)(2)CH2CHMe-; ( RO)(2)PS2-NH4; and R=C2H5, C3H7, i-C3H7;] in a 1: 1 molor ratio in refluxing benzene solution yields low melting solids and light-yellow oily liquids of the type [( RO)(2)PS2R' and OGOPS(2)R', where R' = CH2COOH and Cl2CCOOH], which are hygroscopic in nature. These newly synthesized complexes have been characterized by physicochemical and spectroscopic techniques ( MW, IR, H-1, and (PNMR)-P-31) On the basis of the previously discussed studies, the formation of a P-S-C chemical bond has been established.
  • SOLOZHENKIN, P. M.;YUNUSOV, M. M.;VOLOVICH, T. R.;ZAXAROVA, R. M.;MAXORTO+, DOKL. AN TADZHSSR, 32,(1989) N, S. 251-255
    作者:SOLOZHENKIN, P. M.、YUNUSOV, M. M.、VOLOVICH, T. R.、ZAXAROVA, R. M.、MAXORTO+
    DOI:——
    日期:——
  • Synthesis and Biological Activities of O, O-Dialkyl-dithiophosphoryl-S-acetoxy Triazolo Compounds
    作者:Wen-Bin Chen、Gui-Yu Jin
    DOI:10.1080/10426500307939
    日期:2003.2.1
    In this article, we introduce organic phosphorus moiety into triazole ring to prepare O-dialkyl-dithiophosphoryl-S-acetoxy triazolo compounds and characterize their structures by elementary analysis and (HNMR)-H-1 and IR spectral data. From the results of biological activity screening, we found that the O-dialkyl-dithiophosphoryl-S-acetoxy triazolo compounds show lower fungicidal activities and their structures need to be optimized for the better.
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