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N,N-di-n-butyl-4-methoxyphenylphosphonoamide chloride | 154062-42-7

中文名称
——
中文别名
——
英文名称
N,N-di-n-butyl-4-methoxyphenylphosphonoamide chloride
英文别名
N-butyl-N-[chloro-(4-methoxyphenyl)phosphoryl]butan-1-amine
N,N-di-n-butyl-4-methoxyphenylphosphonoamide chloride化学式
CAS
154062-42-7
化学式
C15H25ClNO2P
mdl
——
分子量
317.796
InChiKey
GVKJBOIGIAPCFJ-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):
    4.4
  • 重原子数:
    20
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Arylphosphonodiamide compounds and herbicidal compositions thereof
    摘要:
    除草剂的化学式为## STR1##其中R为氢,单或多卤素,单或双(C.sub.1-C.sub.4烷基),C.sub.1-C.sub.4烷氧基,C.sub.1-C.sub.4卤代烷氧基,苯氧基或硝基; R.sub.1为氢或C.sub.1-C.sub.4烷基; R.sub.3为C.sub.1-C.sub.6烷基; R.sub.2为C.sub.2-C.sub.4烷基,C.sub.3-C.sub.6环烷基,苯基,可以选择用C.sub.1-C.sub.4烷基,C.sub.1-C.sub.4卤代烷基,C.sub.1-C.sub.4卤代烷氧基,一个或多个卤素或两个C.sub.1-C.sub.4烷氧基,或者一个C.sub.1-C.sub.4烷基和一个C.sub.1-C.sub.4烷氧基,苯基-(C.sub.1-C.sub.2)烷基或吡啶基进行取代; 或者R.sub.1和R.sub.2,和/或R.sub.3和R.sub.4分别与氮原子一起形成一个4-8成员环,可以包括一个氧杂原子;并且R.sub.4为C.sub.1-C.sub.6烷基,C.sub.3-C.sub.6环烷基,苯基,可以选择用C.sub.1-C.sub.4烷基,C.sub.1-C.sub.4卤代烷基,C.sub.1-C.sub.4卤代烷氧基,一个或多个卤素或两个C.sub.1-C.sub.4烷氧基,或者一个C.sub.1-C.sub.4烷基和一个C.sub.1-C.sub.4烷氧基,苯基-(C.sub.1-C.sub.2烷基)或吡啶基; 前提是如果R.sub.1为氢,则R.sub.2为烷基或环烷基。
    公开号:
    US05186733A1
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文献信息

  • US5186733A
    申请人:——
    公开号:US5186733A
    公开(公告)日:1993-02-16
  • Arylphosphonodiamide compounds and herbicidal compositions thereof
    申请人:Imperial Chemical Industries PLC
    公开号:US05186733A1
    公开(公告)日:1993-02-16
    Herbicides have the formula ##STR1## in which R is hydrogen, mono- or poly-halo, mono- or di-(C.sub.1 -C.sub.4 alkyl), C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, phenoxy or nitro; R.sub.1 is hydrogen or C.sub.1 -C.sub.4 alkyl; R.sub.3 is C.sub.1 -C.sub.6 alkyl; R.sub.2 is C.sub.2 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2)alkyl or pyridyl; or R.sub.1 and R.sub.2, and/or R.sub.3 and R.sub.4 respectively, taken together with the nitrogen atom, form a 4-8 member ring, optionally including an oxygen heteroatom; and R.sub.4 is C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2 alkyl) or pyridyl; provided that if R.sub.1 is hydrogen, R.sub.2 is alkyl or cycloalkyl.
    除草剂的化学式为## STR1##其中R为氢,单或多卤素,单或双(C.sub.1-C.sub.4烷基),C.sub.1-C.sub.4烷氧基,C.sub.1-C.sub.4卤代烷氧基,苯氧基或硝基; R.sub.1为氢或C.sub.1-C.sub.4烷基; R.sub.3为C.sub.1-C.sub.6烷基; R.sub.2为C.sub.2-C.sub.4烷基,C.sub.3-C.sub.6环烷基,苯基,可以选择用C.sub.1-C.sub.4烷基,C.sub.1-C.sub.4卤代烷基,C.sub.1-C.sub.4卤代烷氧基,一个或多个卤素或两个C.sub.1-C.sub.4烷氧基,或者一个C.sub.1-C.sub.4烷基和一个C.sub.1-C.sub.4烷氧基,苯基-(C.sub.1-C.sub.2)烷基或吡啶基进行取代; 或者R.sub.1和R.sub.2,和/或R.sub.3和R.sub.4分别与氮原子一起形成一个4-8成员环,可以包括一个氧杂原子;并且R.sub.4为C.sub.1-C.sub.6烷基,C.sub.3-C.sub.6环烷基,苯基,可以选择用C.sub.1-C.sub.4烷基,C.sub.1-C.sub.4卤代烷基,C.sub.1-C.sub.4卤代烷氧基,一个或多个卤素或两个C.sub.1-C.sub.4烷氧基,或者一个C.sub.1-C.sub.4烷基和一个C.sub.1-C.sub.4烷氧基,苯基-(C.sub.1-C.sub.2烷基)或吡啶基; 前提是如果R.sub.1为氢,则R.sub.2为烷基或环烷基。
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