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S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea

中文名称
——
中文别名
——
英文名称
S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea
英文别名
methyl N-methyl-N'-nitro-N-(trichloromethylsulfanyl)carbamimidothioate
S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea化学式
CAS
——
化学式
C4H6Cl3N3O2S2
mdl
——
分子量
298.602
InChiKey
PHXPFTZXPXYBPF-BAQGIRSFSA-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):
    3.5
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    112
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    参考文献:
    名称:
    Substituted guanidine derivatives, their preparation and use
    摘要:
    新型替代硝基胍衍生物及其盐具有以下结构式:##STR1## 其中R.sup.1是取代或未取代的杂环基团;R.sup.2是通过硫原子连接的基团,通过磷原子连接的基团,氰基,--CO--OR.sup.6,其中R.sup.6是取代或未取代的碳氢基团或取代或未取代的杂环基团,或--CO--NR.sup.7 R.sup.8,其中R.sup.7和R.sup.8,相同或不同,各自独立地是氢、取代或未取代的碳氢基团或取代或未取代的杂环基团,或R.sup.7和R.sup.8,与它们连接的氮原子一起构成一个环状氨基团;R.sup.3是氢、取代或未取代的碳氢基团(除了一个在结合位点上取代了氧代基的基团)、通过硫原子连接的基团,通过磷原子连接的基团,氰基,--CO--R.sup.9,其中R.sup.9是氢、取代或未取代的碳氢基团或取代或未取代的杂环基团,--CO--OR.sup.10,其中R.sup.10是取代或未取代的碳氢基团或取代或未取代的杂环基团,或--CO--NR.sup.11 R.sup.12,其中R.sup.11和R.sup.12,相同或不同,各自独立地是氢、取代或未取代的碳氢基团或取代或未取代的杂环基团,或R.sup.11和R.sup.12,与它们连接的氮原子一起构成一个环状氨基团;和R.sup.4是氢或低碳基团;这些化合物具有意外强大的杀虫活性和极低的毒性。
    公开号:
    US05256679A1
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文献信息

  • Novel substituted guanidine derivatives, their preparation and use
    申请人:Takeda Chemical Industries, Ltd.
    公开号:EP0471372A1
    公开(公告)日:1992-02-19
    Novel substituted nitroguanidine derivatives and salts thereof having the following formula: wherein R¹ is a substituted or unsubstituted heterocyclic group; R² is a group attached through a sulfur atom, a group attached through a phosphorus atom, cyano, -CO-OR⁶ wherein R⁶ is a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or -CO-NR⁷R⁸ wherein R⁷ and R⁸, which are the same or different, are each independently hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or R⁷ and R⁸, taken together with the nitrogen atom to which they are attached are a cyclic amino group; R³ is hydrogen, a substituted or unsubstituted hydrocarbon group (except for one substituted with an oxo group at the binding site), a group attached through a sulfur atom, a group attached through a phosphorus atom, cyano, -CO-R⁹ wherein R⁹ is hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, -CO-OR¹⁰ wherein R¹⁰ is a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or -CO-NR¹¹R¹² wherein R¹¹ and R¹², which are the same or different, are each independently hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or R¹¹ and R¹², taken together with the nitrogen atom to which they are attached are a cyclic amino group; and R⁴ is hydrogen or a lower alkyl group; which have unexpectedly potent pesticidal activity and very low toxicity.
    具有下式的新型取代硝基胍衍生物及其盐类: 其中 R¹ 是取代或未取代的杂环基团;R² 是通过硫原子连接的基团、通过磷原子连接的基团、氰基、-CO-OR⁶ 其中 R⁶ 是取代或未取代的烃基或取代或未取代的杂环基,或 -CO-NR⁷R⁸ 其中 R⁷ 和 R⁸、相同或不同,各自独立地为氢、取代或未取代的烃基或取代或未取代的杂环基,或 R⁷ 和 R⁸ 与它们所连接的氮原子一起为环状氨基;R³ 是氢、取代或未取代的烃基(在结合位点被氧代基团取代的除外)、通过硫原子连接的基团、通过磷原子连接的基团、氰基、-CO-R⁹,其中 R𠞙 是氢、取代或未取代的烃基或取代或未取代的杂环基团、-CO-OR¹⁰,其中 R¹⁰ 是取代或未取代的烃基或取代或未取代的杂环基,或-CO-NR¹R¹²,其中 R¹¹ 和 R¹² (相同或不同)各自独立地是氢、取代或未取代的烃基或取代或未取代的杂环基,或 R¹¹ 和 R¹² 与它们所连接的氮原子一起是环状氨基;和 R⁴ 是氢或低级烷基;它们具有意想不到的强杀虫活性和极低的毒性。
  • US5256679A
    申请人:——
    公开号:US5256679A
    公开(公告)日:1993-10-26
  • Substituted guanidine derivatives, their preparation and use
    申请人:Takeda Chemical Industries, Ltd.
    公开号:US05256679A1
    公开(公告)日:1993-10-26
    Novel substituted nitroguanidine derivatives and salts thereof having the following formula: ##STR1## wherein R.sup.1 is a substituted or unsubstituted heterocyclic group; R.sup.2 is a group attached through a sulfur atom, a group attached through a phosphorus atom, cyano, --CO--OR.sup.6 wherein R.sup.6 is a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or --CO--NR.sup.7 R.sup.8 wherein R.sup.7 and R.sup.8, which are the same or different, are each independently hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or R.sup.7 and R.sup.8, taken together with the nitrogen atom to which they are attached are a cyclic amino group; R.sup.3 is hydrogen, a substituted or unsubstituted hydrocarbon group (except for one substituted with an oxo group at the binding site), a group attached through a sulfur atom, a group attached through a phosphorus atom, cyano, --CO--R.sup.9 wherein R.sup.9 is hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, --CO--OR.sup.10 wherein R.sup.10 is a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or --CO--NR.sup.11 R.sup.12 wherein R.sup.11 and R.sup.12, which are the same or different, are each independently hydrogen, a substituted or unsubstituted hydrocarbon group or a substituted or unsubstituted heterocyclic group, or R.sup.11 and R.sup.12, taken together with the nitrogen atom to which they are attached are a cyclic amino group; and R.sup.4 is hydrogen or a lower alkyl group; which have unexpectedly potent pesticidal activity and very low toxicity.
    新型替代硝基胍衍生物及其盐具有以下结构式:##STR1## 其中R.sup.1是取代或未取代的杂环基团;R.sup.2是通过硫原子连接的基团,通过磷原子连接的基团,氰基,--CO--OR.sup.6,其中R.sup.6是取代或未取代的碳氢基团或取代或未取代的杂环基团,或--CO--NR.sup.7 R.sup.8,其中R.sup.7和R.sup.8,相同或不同,各自独立地是氢、取代或未取代的碳氢基团或取代或未取代的杂环基团,或R.sup.7和R.sup.8,与它们连接的氮原子一起构成一个环状氨基团;R.sup.3是氢、取代或未取代的碳氢基团(除了一个在结合位点上取代了氧代基的基团)、通过硫原子连接的基团,通过磷原子连接的基团,氰基,--CO--R.sup.9,其中R.sup.9是氢、取代或未取代的碳氢基团或取代或未取代的杂环基团,--CO--OR.sup.10,其中R.sup.10是取代或未取代的碳氢基团或取代或未取代的杂环基团,或--CO--NR.sup.11 R.sup.12,其中R.sup.11和R.sup.12,相同或不同,各自独立地是氢、取代或未取代的碳氢基团或取代或未取代的杂环基团,或R.sup.11和R.sup.12,与它们连接的氮原子一起构成一个环状氨基团;和R.sup.4是氢或低碳基团;这些化合物具有意外强大的杀虫活性和极低的毒性。
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