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2,2,2-trichloro-N-methylacetimidoyl chloride | 57182-16-8

中文名称
——
中文别名
——
英文名称
2,2,2-trichloro-N-methylacetimidoyl chloride
英文别名
(1Z)-2,2,2-Trichloro-N-methylethanimidoyl chloride;2,2,2-trichloro-N-methylethanimidoyl chloride
2,2,2-trichloro-N-methylacetimidoyl chloride化学式
CAS
57182-16-8
化学式
C3H3Cl4N
mdl
——
分子量
194.876
InChiKey
WGBRKOAOIAXHRL-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:
    173.2±40.0 °C(Predicted)
  • 密度:
    1.53±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    12.4
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

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文献信息

  • Reactions of N-alkyl- and N-aryltrihalogenoacetamides with phosphorus pentachloride
    作者:A. D. Sinitsa、A. A. Shalimov、A. M. Nesterenko、D. M. Malenko
    DOI:10.1007/s11172-005-0316-2
    日期:2005.3
    the study of reactions of N-alkyl- and N-aryltrihalogenoacetamides with PCl5, it was demonstrated for the first time that 3-alkyl(aryl)-2,2,2,4 tetrachloro-4-trihalomethyl-1,3,2-λ5-oxazaphosphetanes are intermediates in the synthesis of trihaloacetimidoyl chlorides. According to quantum-chemical calculations, acyclic N-tetrachlorophosphoranes, which are the primary products in the reactions of trihaloacetamides
    在 N-烷基-和 N-芳基三卤代乙酰胺与 PCl5 反应的研究中,首次证明了 3-烷基(芳基)-2,2,2,4 四氯-4-三卤甲基-1,3,2 -λ5-oxazaphosphetanes 是合成三卤代乙酰亚氨基酰氯的中间体。根据量子化学计算,三卤乙酰胺与 PCl5 反应的主要产物无环 N-四氯正膦快速环化为相应的磷酸酯,随后 1,3- 氯代迁移产生具有五配位 P 的氧氮杂膦原子。
  • Goerdeler,J. et al., Chemische Berichte, 1975, vol. 108, p. 3071 - 3078
    作者:Goerdeler,J. et al.
    DOI:——
    日期:——
  • Sinitsa, A. D.; Krishtal', V. S.; Kal'chenko, V. I., Journal of general chemistry of the USSR, 1980, vol. 50, # 6, p. 1042 - 1046
    作者:Sinitsa, A. D.、Krishtal', V. S.、Kal'chenko, V. I.
    DOI:——
    日期:——
  • Boehme,H. et al., Liebigs Annalen der Chemie, 1979, p. 1447 - 1455
    作者:Boehme,H. et al.
    DOI:——
    日期:——
  • Sinitsa, A. D.; Krishtal', V. S.; Kal'chenko, V. I., Journal of general chemistry of the USSR, 1980, vol. 50, # 10, p. 1943 - 1946
    作者:Sinitsa, A. D.、Krishtal', V. S.、Kal'chenko, V. I.、Markovskii, L. N.
    DOI:——
    日期:——
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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