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2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate

中文名称
——
中文别名
——
英文名称
2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate
英文别名
Bis(1,1,2,2,2-pentafluoroethyl)phosphinate;[dimethylamino(methoxy)methylidene]-dimethylazanium;bis(1,1,2,2,2-pentafluoroethyl)phosphinate;[dimethylamino(methoxy)methylidene]-dimethylazanium
2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate化学式
CAS
——
化学式
C4F10O2P*C6H15N2O
mdl
——
分子量
432.198
InChiKey
FLECSSLEPQECIG-UHFFFAOYSA-M
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):
    2.76
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    55.6
  • 氢给体数:
    0
  • 氢受体数:
    13

反应信息

  • 作为产物:
    描述:
    甲醇tris(pentafluoroethyl)phosphine oxide1,1,3,3-四甲基脲乙二醇二甲醚 为溶剂, 反应 5.0h, 以91.9%的产率得到2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate
    参考文献:
    名称:
    [DE] IONISCHE FLÜSSIGKEITEN MIT URONIUM- ODER THIOURONIUM-KATIONEN
    [EN] IONIC LIQUID COMPRISING URONIUM CATIONS OR THIOURONIUM CATIONS
    [FR] LIQUIDES IONIQUES CONTENANT DES CATIONS D'URONIUM OU DE THIOURONIUM
    摘要:
    这项发明涉及具有硫脲或尿素阳离子的盐,它们的制备方法以及它们作为离子液体的用途。
    公开号:
    WO2004106287A1
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文献信息

  • PROCESS FOR THE PREPARATION OF PHOSPHINIC ACID ESTERS
    申请人:MERCK PATENT GmbH
    公开号:US20150045572A1
    公开(公告)日:2015-02-12
    The invention relates to a process for the preparation of alkyl phosphinates, alkenyl phosphinates, alkynyl phosphinates or phenyl phosphinates by reaction of a corresponding phosphine oxide with an alcohol or phenol in the presence of alkali-metal fluoride or tetraalkylammonium fluoride.
    该发明涉及一种通过将相应的膦氧化物与醇或在碱化物或四烷基化物存在下反应制备烷基膦酸酯、烯基膦酸酯、炔基膦酸酯或苯基膦酸酯的过程。
  • Process for the preparation of organic salts containing bis(perfluoroalkyl) phosphinate anions
    申请人:Ignatyev Mykola Nikolai
    公开号:US20070128515A1
    公开(公告)日:2007-06-07
    The invention relates to a method for the production of organic salts containing bis(perfluoroalkyl)phosphinate anions. According to said method, a tris(perfluoroalkyl)phosphine oxide is reacted with an alcohol and an organic base, which is stronger than the alcohol. The invention also relates to the salts which are produced according to said method and to the use thereof as ionic liquids.
    本发明涉及一种制备含有双(全氟烷基)膦酸盐阴离子的有机盐的方法。根据该方法,三(全氟烷基)膦氧化物与一种醇和一种比醇更强的有机碱反应。本发明还涉及根据该方法制备的盐以及将其用作离子液体的用途。
  • IONISCHE FLÜSSIGKEITEN MIT URONIUM- ODER THIOURONIUM-KATIONEN
    申请人:Merck Patent GmbH
    公开号:EP1628952A1
    公开(公告)日:2006-03-01
  • VERFAHREN ZUR HERSTELLUNG VON ORGANISCHEN SALZEN MIT BIS(PERFLUORALKYL)PHOSPHINAT-ANIONEN
    申请人:Merck Patent GmbH
    公开号:EP1685095B1
    公开(公告)日:2010-08-11
  • VERFAHREN ZUR HERSTELLUNG VON PHOSPHINSÄUREESTERN
    申请人:Merck Patent GmbH
    公开号:EP2820026B1
    公开(公告)日:2016-01-13
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同类化合物

氯(双五氟乙基)膦 5-萘-2-基-1,3-噁唑 1-氯-2-[2-氯乙基(甲基)磷基]乙烷 1-丁基-1-甲基吡咯烷鎓三(五氟乙基)三氟磷酸盐 1,1,1,3,3,3-六氟-2-(2,2,2-三氟-1-羟基-1-(三氟甲基)乙基磷酰基)-2-丙醇 bis(pentafluoroethyl)phosphinyl amide 1-butylpyridinium bis(pentafluoroethyl)phosphinate N,N-butylmethylpyrrolidinium bis(pentafluoroethyl)-phosphinate bis(pentafluoroethyl)phosphinate anion triethylmethylammonium bis(pentafluoroethyl)-phosphinate bis(dimethylamino)chlorocarbenium bis(pentafluorethyl)phosphinate 1-methyl-1-propargylpyrrolidinium bis(pentafluoro-ethyl)phosphinate N,N-dimethylpyrrolidinium bis(pentafluoroethyl)-phosphinate 1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate propargyl bis(pentafluoroethyl)phosphinate 1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate 1-propargyl-3-methylimidazolium bis(pentafluoroethyl)-phosphinate 1-ethyl-3-methylimidazolium bis(nonafluorobutyl)-phosphinate tetrabutylammonium tris(pentafluoroethyl)trifluorophosphate bis-(2,2-dichloro-1-hydroxy-ethyl)-phosphinic acid 2,2,3,3,4,4,5,5-octafluoropentyl bis(pentafluoroethyl) phosphinate 2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate ethyl bis(nonafluorobutyl)phosphinate fluorobis(pentafluoroethyl)phosphane tetraethylammonium bis(nonafluorobutyl)tetrafluorophosphate tetraethylammonium tris(pentafluoroethyl)trifluorophosphate tris(pentafluoroethyl)phosphane ethyl bis(pentafluoroethyl)phosphinate N,N,N',N'-tetramethyl-N''-ethylguanidinium bis(pentafluoroethyl)phosphinate 3-bromopropyl bis(pentafluoroethyl)phosphinate Tetramethylammonium tris(pentafluorophosphate Bis-(2-chlor-ethyl)-thiophosphinsaeure-ethylester ethyl bis(pentafluoroethyl)phosphinite Bis-heptafluorpropyl-fluorphosphin trimethylsilyl bis(pentafluoroethyl)phosphinite tris(undecafluoroisopentyl)phosphine oxide 1-(Bis-undecafluoropentyl-phosphinoyl)-1,1,2,2,3,3,4,4,5,5,5-undecafluoro-pentane Bis-(2-chlor-ethyl)-chlorphosphin 1,1,1,3,3,3,1',1',1',3',3',3'-dodecafluoro-2,2'-phosphanediyl-bis-propan-2-ol Bis-<2-chlor-aethyl>-chlormethyl-phosphinoxid Tri(β-chlorethyl)phosphinoxid cis-[(C2F5)2P(methyl)]4Pt Perfluorhexylphosphinsaeure bis-(2,2,2-trichloro-1-hydroxy-ethyl)-phosphinic acid ethyl ester bis(pentafluoroethyl)phosphinyl bromide (S)-4-benzyl-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4,5-dihydrooxazole (S)-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4-phenyl-4,5-dihydrooxazole tetra(n-butyl)phosphonium tris(pentafluoroethyl)trifluorophosphate silver bis(heptafluoropropyl)phosphinate Tris(2,2,3,3,4,4,5,5-octafluoropentyl)phosphine