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N-isopropyl dichloroacetimidoyl chloride | 79166-98-6

中文名称
——
中文别名
——
英文名称
N-isopropyl dichloroacetimidoyl chloride
英文别名
N-isopropyldichloroacetimidoyl chloride;2,2-dichloro-N-propan-2-ylethanimidoyl chloride
N-isopropyl dichloroacetimidoyl chloride化学式
CAS
79166-98-6
化学式
C5H8Cl3N
mdl
——
分子量
188.484
InChiKey
NAFZIDSHKMQJRH-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:
    9
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    12.4
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    N-isopropyl dichloroacetimidoyl chloride3,5-二氯苯胺丙酮 为溶剂, 以92.7%的产率得到N-isopropyldichloroacetimidoyl chloride N-3',5'-Dichlorophenyl-N'-isopropyldichloroacetamidine
    参考文献:
    名称:
    Haloacetamidines and the herbicidal use thereof
    摘要:
    二氯乙酰胺亚胺的化学式为##STR1##其中A和B分别选自氢、氟、氯、溴和甲基,但至少A或B之一不是氢;M为氢或甲基;X选自三氟甲基、低碳基、硝基、氯、溴、氟、氰基、低碳氧基乙酰基、低碳硫基、三氟甲基硫基和3,3-二低碳基脲基;Y选自氢、低碳基、氯、氟、硝基、三氟甲基和低碳氧基;Z选自氢和氯;R.sub.1选自氢、烷基和烯丙基;R.sub.2选自烷基、烯丙基、苄基、羟基烷基、炔基、N-烷基酰胺、烷氧基烷基、二烷氧基烷基、烷氧基、氰基烷基、取代苯基,其中取代基选自三氟甲基、二氯甲基和3,3-二甲基脲基;R.sub.1和R.sub.2连同氮原子选自烷基取代的噁唑基、吗啉基、哌啶基和吡咯啉基;以及其盐;可用作除草剂。
    公开号:
    US04670593A1
  • 作为产物:
    描述:
    N-Isopropyl-2,2-dichloroacetamide盐酸三氯氧磷五氯化磷 为溶剂, 以gave 360 grams (65% yield) of N-isopropyldichloroacetimidoyl chloride, b.p. 63°-72° C.的产率得到N-isopropyl dichloroacetimidoyl chloride
    参考文献:
    名称:
    Haloacetamidines compositions and the herbicidal use thereof
    摘要:
    具有以下式子的二氯乙酰胺类化合物:##STR1## 其中A和B独立地选自氢、氟、氯、溴和甲基,但至少其中一个不是氢;M为氢或甲基;X选自三氟甲基、低碳基、硝基、氯、溴、氟、氰、低碳氧乙酰基、低碳硫基、三氟甲基硫基和3,3-二低碳基脲基;Y选自氢、低碳基、氯、氟、硝基、三氟甲基和低碳氧基;Z选自氢和氯;R.sub.1选自氢、烷基和烯丙基;R.sub.2选自烷基、烯丙基、苄基、羟基烷基、炔基、N-烷基酰胺基、烷氧基烷基、二烷氧基烷基、烷氧基、氰基烷基、取代苯基,其中取代基选自三氟甲基、二氯和3,3-二甲基脲基;R.sub.1和R.sub.2与氮一起被选自烷基取代的噁唑烷基、吗啉基、哌啶基和吡咯烷基的群体中;以及它们的盐;作为除草剂有用。
    公开号:
    US04781752A1
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文献信息

  • Dichloromethyl oxadiazole herbicide antidotes
    申请人:Stauffer Chemical Company
    公开号:US04488897A1
    公开(公告)日:1984-12-18
    A novel class of 2-dichloromethyl-5-phenyl or substituted phenyl 1,3,4-oxadiazole compounds having the formula ##STR1## wherein R is unsubstituted phenyl or phenyl mono-, di-, or tri-substituted with halogen, hydroxy or nitro, which are useful as antidotes for thiocarbamate herbicidal crop injury.
    一种新型的2-二氯甲基-5-苯基或取代苯基1,3,4-噁二唑化合物,其化学式为##STR1##其中R是未取代的苯基或卤素、羟基或硝基单、二或三取代的苯基,可用作对硫代氨基甲酸酯除草剂对作物的损伤的解毒剂。
  • Haloacetamidines and the herbicidal use thereof
    申请人:Stauffer Chemical Co.
    公开号:US04670593A1
    公开(公告)日:1987-06-02
    Dichloroacetamidines having the formula ##STR1## in which A and B are independently selected from hydrogen, fluorine, chlorine, bromine and methyl, provided that at least one of A or B is other than hydrogen; M is hydrogen or methyl; X is selected from the group consisting of trifluoromethyl, lower alkyl, nitro, chloro, bromo, fluoro, cyano, lower alkoxy acetyl, lower alkylthio, trifluoromethylthio, and 3,3-diloweralkyl ureido; Y is selected from the group consisting of hydrogen, lower alkyl, chloro, fluoro, nitro, trifluoromethyl, and lower alkoxy; Z is selected from the group consisting of hydrogen and chloro; R.sub.1 is selected from the group consisting of hydrogen, alkyl and allyl; R.sub.2 is selected from the group consisting of alkyl, allyl, benzyl, hydroxyalkyl, alkynyl, N-alkyl amido, alkoxyalkyl, dialkoxyalkyl, alkoxy, cyano alkyl, substituted phenyl wherein the substituent is selected from the group trifluoromethyl, dichloro and 3,3-dimethylureido; and R.sub.1 and R.sub.2 taken together with the nitrogen is selected from the group consisting of alkyl substituted oxazolidyl, morpholinyl, piperidinyl and pyrrolidinyl; and salts thereof; useful as herbicides.
    二氯乙酰胺亚胺的化学式为##STR1##其中A和B分别选自氢、氟、氯、溴和甲基,但至少A或B之一不是氢;M为氢或甲基;X选自三氟甲基、低碳基、硝基、氯、溴、氟、氰基、低碳氧基乙酰基、低碳硫基、三氟甲基硫基和3,3-二低碳基脲基;Y选自氢、低碳基、氯、氟、硝基、三氟甲基和低碳氧基;Z选自氢和氯;R.sub.1选自氢、烷基和烯丙基;R.sub.2选自烷基、烯丙基、苄基、羟基烷基、炔基、N-烷基酰胺、烷氧基烷基、二烷氧基烷基、烷氧基、氰基烷基、取代苯基,其中取代基选自三氟甲基、二氯甲基和3,3-二甲基脲基;R.sub.1和R.sub.2连同氮原子选自烷基取代的噁唑基、吗啉基、哌啶基和吡咯啉基;以及其盐;可用作除草剂。
  • Haloacetamidines compositions and the herbicidal use thereof
    申请人:Stauffer Chemical Company
    公开号:US04781752A1
    公开(公告)日:1988-11-01
    Dichloroacetamidines having the formula ##STR1## in which A and B are independently selected from hydrogen, fluorine, chlorine, bromine and methyl, provided that at least one of A or B is other than hydrogen; M is hydrogen or methyl; X is selected from the group consisting of trifluoromethyl, lower alkyl, nitro, chloro, bromo, fluoro, cyano, lower alkoxy acetyl, lower alkylthio, trifluoromethylthio, and 3,3-diloweralkyl ureido; Y is selected from the group consisting of hydrogen, lower alkyl, chloro, fluoro, nitro, trifluoromethyl, and lower alkoxy; Z is selected from the group consisting of hydrogen and chloro; R.sub.1 is selected from the group consisting of hydrogen, alkyl and allyl; R.sub.2 is selected from the group consisting of alkyl, allyl, benzyl, hydroxyalkyl, alkynyl, N-alkyl amido, alkoxyalkyl, dialkoxyalkyl, alkoxy, cyano alkyl, substituted phenyl wherein the substituent is selected from the group trifluoromethyl, dichloro and 3,3-dimethylureido; and R.sub.1 and R.sub.2 taken together with the nitrogen is selected from the group consisting of alkyl substituted oxazolidyl, morpholinyl, piperidinyl and pyrrolidinyl; and salts thereof; useful as herbicides.
    具有以下式子的二氯乙酰胺类化合物:##STR1## 其中A和B独立地选自氢、氟、氯、溴和甲基,但至少其中一个不是氢;M为氢或甲基;X选自三氟甲基、低碳基、硝基、氯、溴、氟、氰、低碳氧乙酰基、低碳硫基、三氟甲基硫基和3,3-二低碳基脲基;Y选自氢、低碳基、氯、氟、硝基、三氟甲基和低碳氧基;Z选自氢和氯;R.sub.1选自氢、烷基和烯丙基;R.sub.2选自烷基、烯丙基、苄基、羟基烷基、炔基、N-烷基酰胺基、烷氧基烷基、二烷氧基烷基、烷氧基、氰基烷基、取代苯基,其中取代基选自三氟甲基、二氯和3,3-二甲基脲基;R.sub.1和R.sub.2与氮一起被选自烷基取代的噁唑烷基、吗啉基、哌啶基和吡咯烷基的群体中;以及它们的盐;作为除草剂有用。
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同类化合物

溴甲烯基二甲基溴化铵 全氟(5-氮杂-4-壬烯) N-((5-溴-3-甲氧基-2H-吡咯-2-基)甲基)-n-乙基乙胺 2,2,3,4,5-五氯吡咯 (氯亚甲基)二甲基氯化铵 dibutyl(chloromethylene)ammonium chloride N-(methoxycarbonyl)trifluoroacetimidoyl chloride Vilsmeier's reagent Vilsmeier reagent N,N-diethylchloromethyleneiminium chloride (Bromomethylene)diethylammonium bromide 3,6-dichloro-2,5-dihydro-pyrazine chloroformiminium chloride N-Cyclohexyl-acetimidoylfluorid 2,2,4,5-Tetrachlor-2H-imidazol N-(2-Chloro-1-methyl-ethyl)-acetimidoyl chloride N-tert-Butyl-2-chloro-acetimidoyl chloride acetimidoyl chloride N-Allyl-2,2-dimethyl-propionimidoyl chloride Bromessigsaeure-bromid-imid 4-tetrafluoropyridyl silver(I) 2-chloro-N-(2-cyanoethyl)ethanimidoyl chloride N-Cyclohexyl-acetimidoylchlorid 3-fluoro-2,2-bis-trifluoromethyl-2H-azirine perfluoro[(ethyl)(ethylidene)amine] N1,N2-Bis-((S)-1-chloromethyl-2-methyl-propyl)-oxalodiimidoyl dichloride 1-(1-Chlor-ethylidenamino)-isobuten ClC(CF3)N(n-C6H13) N-(cyclohexyl)-2,2,2-trifluoroacetimidoyl chloride N,N'-dihexyloxalimide dichloride 2-ethyl-N-butyl-hexaneimidoyl chloride N,3,3-Trimethylbutanimidoylchlorid 2-bromo-N,2-dimethylpropanimidoyl chloride Perfuor-(2-methy-2H-azirin) 1-aza-2-chloro-ethene propionimidoyl chloride N-(1-adamantyl)ethanimidoyl chloride N-(n-Octyl)-2,2,2-trifluoroacetimidoyl chloride N-Ethyl-pivalimidsaeurechlorid N-(2-Bromo-1,1,2,2-tetrafluoro-ethyl)-2,2,2-trifluoro-acetimidoyl fluoride 2,3,5,6-tetrachloro-4-pyridyllithium Pentanimidoyl fluoride Cyanformimidchlorid Chloromethylidene(dimethyl)azanium;dichlorooxy(oxo)phosphanium 2,2,3-Trifluoro-2H-azirene (1Z)-2,2-Dichloro-N-propylethanimidoyl chloride Cyanomethanimidoyl fluoride Methanimidoyl fluoride 1,2,4,5,6-Pentafluoro-3-azabicyclo<4.2.0>okta-2,4-dien 2,4-Difluoro-3-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)azete