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N-(n-Octyl)-2,2,2-trifluoroacetimidoyl chloride | 172510-99-5

中文名称
——
中文别名
——
英文名称
N-(n-Octyl)-2,2,2-trifluoroacetimidoyl chloride
英文别名
N-Octyl-trifluor-acetimidoylchlorid;Ethanimidoyl chloride, 2,2,2-trifluoro-N-octyl-;2,2,2-trifluoro-N-octylethanimidoyl chloride
N-(n-Octyl)-2,2,2-trifluoroacetimidoyl chloride化学式
CAS
172510-99-5
化学式
C10H17ClF3N
mdl
——
分子量
243.7
InChiKey
WHHGGOLFHBLSQJ-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:
    214.2±50.0 °C(Predicted)
  • 密度:
    1.10±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    12.4
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:6750323344e69055277e84089f93e47b
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反应信息

  • 作为反应物:
    描述:
    N-(n-Octyl)-2,2,2-trifluoroacetimidoyl chloride一水合肼二甲基亚砜 作用下, 反应 20.33h, 生成 (4-octyl-5-(trifluoromethyl)-4H-1,2,4-triazol-3-yl)(phenyl)methanone
    参考文献:
    名称:
    通过三氟乙酰氨基酰肼和甲基酮的无金属环化合成 5-三氟甲基-1,2,4-三唑
    摘要:
    已经实现了一种通过 I 2介导的 [4+1] 环化容易获得的三氟乙酰氨基酰肼和甲基酮来合成 5-三氟甲基-1,2,4-三唑的无金属方法。该转化包括碘化/Kornblum 氧化、分子间脱水缩合和碘介导的分子内环化/芳香化序列。开发的协议可以很容易地扩展到 3 mmol 规模而不会明显降低效率,并且可以通过连续的一锅方式实施。
    DOI:
    10.1002/adsc.202100130
  • 作为产物:
    参考文献:
    名称:
    The Formation of Tetrazoles by the Condensation of Organic Azides with Nitriles
    摘要:
    DOI:
    10.1021/jo01053a043
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文献信息

  • Studies on Organophosphorus Compounds 92: A Facile Synthesis of 1-Substituted 5-Trifluoromethylimidazole-4-phosphonates
    作者:Weisheng Huang、Chengye Yuan
    DOI:10.1055/s-1996-4243
    日期:1996.4
    Base-induced cycloaddition of diethyl isocyanomethylphosphonate to trifluoroacetimidoyl chlorides gives 1-substituted diethyl 5-trifluoromethylimidazole-4-phosphonates with high regioselectivity.
    在碱诱导下,异甲基膦酸二乙酯与三氟乙酰发生环加成反应,以高区域选择性得到 1-取代的 5-三甲基咪唑-4-膦酸二乙酯
  • An Efficient and Regioselective Synthesis of 1-Aryl(Alkyl)-4-Diethoxyphosphoryl-5-Trifluoromethylimidazoles
    作者:Chengye Yuan、Weisheng Huang
    DOI:10.1080/10426509608545195
    日期:1996.1
    Abstract 1-Substituted-4-diethoxyphosphoryl-5-trifluoromethylimidazoles are prepared regioselectively from diethyl isocyanomethylphosphonate and N-substituted trifluoroacetimidoyl chlorides. The reaction mechanism was discussed.
    摘要 1-取代-4-二乙氧基酰基-5-三甲基咪唑是由异甲基膦酸二乙酯和N-取代的三酰亚胺区域选择性地制备的。讨论了反应机理。
  • Facile synthesis of 1-substituted 5-trifluoromethylimidazole-4-carboxylates
    作者:Wei Sheng Huang、Cheng Ye Yuan、Zhi Qin Wang
    DOI:10.1016/0022-1139(95)03299-s
    日期:1995.10
    Base-induced cycloaddition of ethyl isocyanoacetates to trifluoroacetimidoyl chlorides gives ethyl 5-trifluoromethylimidazole-4-carboxylates with high regioselectivity.
  • Huang, Weisheng; Zhang, Yixin; Yuan, Chengye, Phosphorus, Sulfur and Silicon and the Related Elements, 1995, vol. 107, # 1-4, p. 21 - 26
    作者:Huang, Weisheng、Zhang, Yixin、Yuan, Chengye
    DOI:——
    日期:——
  • A new and simple approach to N-substituted trifluoroacetimidoyl aryl ketones
    作者:Wei Sheng Huang、Cheng Ye Yuan、Zhi Qin Wang
    DOI:10.1016/0022-1139(95)03287-n
    日期:1995.10
    Using 1,3-dimethylimidazolium iodide as a catalyst, the reaction of trifluoroacetimidoyl chloride with an aromatic aldehyde in the presence of sodium hydride gives N-substituted trifluoroacetimidoyl aryl ketones.
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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 3-Difluoromethyl-2,2,3,4,4,4-hexafluoro-N-trifluoromethyl-butyrimidoyl fluoride (Z)-1,5-Dichloro-2,5-dimethyl-hept-1-en-3-yne N-Methyl-bromcarbimino-zinntribromid Bis-(N-methyl-chlorcarbimino)-zinndichlorid 2,4,6,8-tetrafluoro-3,7-bis-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-[1,5]diazocine N-ethyl-S-chloroisothiocarbamoyl chloride 3,4-dichloropentafluoro-2-aza-2-butene N,2-dimethyl-2-chloropropaneimidoyl chloride Tetrachlormalonimidoyldichlorid 2,2-dichloro-3-(2-chloro-3,3-dimethylbutyl)azirine tris(chloro(methylimino)methoxy)tantalum(V) chloride Isobuttersaeure-cyclohexylimidchlorid N-n-Heptyl-S-chlor-isothiocarbamoylchlorid [2-Bromo-2-chloro-1-methyl-prop-(E)-ylidene]-isopropyl-amine N-Butyl-2,2,2-trifluoro-acetimidoyl bromide perchloro-3,5-diaza-2,4-heptadiene N-(2,2-Dichlorethyliden)-trifluormethylamin ((Z)-2-Chloro-propenyl)-diisopropyl-phosphane N-(perfluoro-2-methylcyclopentenyl)chlorosulfanylformimidoyl chloride 2-tert-Butyl-1-chloro-3-((E)-1,3-dichloro-2-methyl-propenyl)-1H-phosphirene 4,6-Difluoro-1,3,5-tris-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-2-aza-bicyclo[2.2.0]hexa-2,5-diene propyl N'-(2,3-dibromopropyl)carbamimidothioate;hydrobromide 1,1,3,3-bis(trimethylene)-2-methyl-5,5-dichloro-1,4-pentadiene Propenylisocyaniddichlorid 3-(Dichloromethylene-carbamoyl)-propionyl chloride dichlorotris(perfluoroisopropylideneamino)phosphorane 1,1-dichloro-N-[1,2,2,2-tetrachloro-1-(dichloromethylideneamino)ethyl]methanimine (+-)-1-(1.4.5.6.7.7-hexachloro-norbornen-(5)-yl-(2endo))-ethanone-(1)-oxime 2,2,3,3,4,4,4-Heptafluor-butyrohydroxamoyl-chlorid 2.2.2-Trifluor-1-trifluormethyl-ethylimino-difluormethan N-butyl-2-chloro-2-fluoro-acetimidoyl fluoride 2-chloro-perfluoro(4-methyl-3-aza-2-pentene) 2,2,2-trifluoro-acetamidine; silver-compound Tetrachlor-<1,2,2,2-tetrachlor-vinylamino>-antimon 2,2,2-trichloro-acetimidoyl bromide; hydrobromide Methyl-(3-chlor-but-2-enyl)-amin 2,3-Dicyano-butanediimidoyl dichloride (1-chloro-butylidene)-dimethyl-ammonium; chloride acetimidoyl iodide; hydriodide perfluoro(3-methyl-2,5-diaza-2,5-hexadiene) N-tert-Butyl-2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoro-heptanimidoyl iodide 2,4,5-trichloro-2-pentachloroethyl-2H-imidazole N-[1,1,1,4,4,5,5,5-octafluoro-2-(trifluoromethyl)pent-2-en-3-yl]oxypropan-2-imine