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bis(pentafluoroethyl)phosphinic acid | 103321-11-5

中文名称
——
中文别名
——
英文名称
bis(pentafluoroethyl)phosphinic acid
英文别名
bis(perfluoroethyl)phosphinic acid;bis(pentafluorethyl)phosphinic acid;bis(1,1,2,2,2-pentafluoroethyl)phosphinic acid
bis(pentafluoroethyl)phosphinic acid化学式
CAS
103321-11-5
化学式
C4HF10O2P
mdl
——
分子量
302.009
InChiKey
YSRVDLQDMZJEDO-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:
    63-64 °C(Press: 0.938 Torr)
  • 密度:
    1.767±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    12

SDS

SDS:c94fd2baaf6bfb73fd04dba7488f14ec
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    bis(pentafluoroethyl)phosphinic acid氯仿五氯化磷 作用下, 反应 2.0h, 以18.4 g的产率得到bis(pentafluoroethyl)phosphinic acid chloride
    参考文献:
    名称:
    光酸発生剤及びフォトリソグラフィー用樹脂組成物
    摘要:
    提供具有高光敏度、优异耐热稳定性,对疏水性材料具有高相容性,且对光刻胶溶剂具有优异溶解性的非离子光酸发生剂。本发明涉及一种非离子光酸发生剂(A),其特征在于它由下式(1)表示。【式(1)中,R1和R2代表具有取代基的炭链基(部分或全部氢原子可能被氟取代) ,其碳数为1~18。R1和R2可以相同,也可以不同。Y代表由式(2)表示的基。】【无图选项】
    公开号:
    JP2015151347A
  • 作为产物:
    描述:
    五氟碘乙烷乙基溴化镁三氯氧磷 作用下, 以 乙醚 为溶剂, 反应 1.0h, 生成 bis(pentafluoroethyl)phosphinic acid
    参考文献:
    名称:
    全氟烷基格氏试剂与磷酰氯和苯基膦酰二氯反应的研究
    摘要:
    全氟烷基格氏试剂在-78°C到室温下与磷酰卤反应,选择性地生成双(全氟烷基)膦酰卤,经水后处理,可以高总收率得到双(全氟烷基)次膦酸。全氟烷基格氏试剂与苯基膦二氯化物 产生高产率的双(全氟烷基)苯基膦氧化物,其易于水解为全氟烷基(苯基)次膦酸。
    DOI:
    10.1039/c2dt31371e
  • 作为试剂:
    描述:
    、 、 tris(pentafluoroethyl)difluorophosphorane 、 在 SiO2 、 (C2F5)3PF2 、 tris(pentafluoroethyl)phosphanebis(pentafluoroethyl)phosphinic acid 作用下, 20.0~120.0 ℃ 、173.32 kPa 条件下, 反应 4.0h, 以Clear and colourless (C2F5)3P═O (6.27 g; 15.5 mmol; 55%) can be isolated in 99% purity的产率得到tris(pentafluoroethyl)phosphane
    参考文献:
    名称:
    Process for the preparation of tris(perfluoroalkyl)phosphine oxides and bis(perfluoroalkyl)phosphinic acids
    摘要:
    本发明涉及一种通过将三(全氟烷基)二氟膦烷或双(全氟烷基)三氟膦烷与非金属氧化物、类金属氧化物或含有碱性氧残基的有机化合物反应制备三(全氟烷基)膦氧化物和双(全氟烷基)膦酸的方法。
    公开号:
    US09346838B2
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文献信息

  • [DE] VERFAHREN ZUR HERSTELLUNG VON GUANIDINIUM-SALZEN<br/>[EN] METHOD FOR PRODUCING GUANIDINIUM SALTS<br/>[FR] PROCEDE DE PRODUCTION DE SELS DE GUANIDINIUM
    申请人:MERCK PATENT GMBH
    公开号:WO2005075413A1
    公开(公告)日:2005-08-18
    Die vorliegende Erfindung betrifft ein zweistufiges Verfahren zur Herstellung von Guanidinium-Salzen der Formel (1), wobei die Substituenten R eine in Anspruch 1 angegebene Bedeutung haben und A- ein Sulfonat, Alkyl- oder Aryl-Sulfat, Hydrogensulfat, Imid, Methanid, Carboxylat, Phosphat, Phosphinat, Phosphonat, Borat, Thiocyanat, Perchlorat, Fluorsilikat oder Nitrat ist, sowie Zwischenverbindungen aus diesem Verfahren.
    This invention relates to a two-step process for the production of guanidinium salts of formula (1), wherein the substituents R have the meaning as defined in claim 1 and A- is a sulfonate, alkyl or aryl sulfate, hydrogen sulfate, imide, methanide, carboxylate, phosphate, phosphinate, phosphonate, borate, thiocyanate, perchlorate, fluorosilicate, or nitrate, as well as intermediates from this process.
  • PROCESS FOR THE PREPARATION OF BIS(FLUOROALKYL)PHOSPHINIC ACID OR FLUOROALKYLPHOSPHONIC ACID
    申请人:Ignatyev Nikolai Mykola
    公开号:US20110130589A1
    公开(公告)日:2011-06-02
    The invention relates to a process for the preparation of bis(fluoroalkyl)phosphinic acid and/or fluoroalkylphosphonic acid by reaction of, monofluoroalkyltetrafluorophosphorane bis(fluoroalkyl)trifluorophosphorane or tris(fluoroalkyl)difluorophosphorane with water.
    该发明涉及通过单氟烷基四氟磷烷、双(氟烷基)三氟磷烷或三(氟烷基)二氟磷烷与水反应制备双(氟烷基)膦酸和/或氟烷基膦酸的过程。
  • Reaction of Perfluoroalkyl Grignard Reagents with Phosphorus Trihalides: A New Route to Perfluoroalkyl-phosphonous and -phosphonic Acids
    作者:Adil I. Hosein、Xavier F. Le Goff、Louis Ricard、Andrew J. M. Caffyn
    DOI:10.1021/ic102063e
    日期:2011.2.21
    with phosphorus(III) halides was explored. In the process a new convenient, one-pot, high yield method for the synthesis of (perfluoroalkyl)phosphonic acids has been developed. Perfluoroalkyl Grignard reagents react with phosphorus trichloride or phosphorus tribromide to form (perfluoroalkyl)phosphonous dihalides. Hydrolysis gives the corresponding (perfluoroalkyl)phosphonous acids. Oxidation of the
    探索了全氟烷基格氏试剂与卤化磷(III)的反应。在该方法中,已经开发了一种新的方便,一锅法,高收率的合成(全氟烷基)膦酸的方法。全氟烷基格氏试剂与三氯化磷或三溴化磷反应生成(全氟烷基)二卤化磷。水解得到相应的(全氟烷基)亚膦酸。基于相应的全氟烷基碘,用H 2 O 2氧化亚膦酸可产生60-78%的总产率的(全氟烷基)膦酸。甲苯鎓盐[MeC 6 H 4 NH 3 ] 2 [C 2报道了F 5 PO 3和[MeC 6 H 4 NH 3 ] [C 8 F 17 P(O)2 OH]。
  • PROCESS FOR THE PREPARATION OF BIS(PERFLUOROALKYL)PHOSPHINIC ACID ANHYDRIDES
    申请人:MERCK PATENT GMBH
    公开号:US20140155649A1
    公开(公告)日:2014-06-05
    The invention relates to a process for the preparation of bis(perfluoroalkyl)phosphinic acid anhydrides by reaction of a bis(perfluoroalkyl)phosphinic acid with phosphorus pentoxide, to novel bis(perfluoroalkyl)phosphinic acid anhydrides and to uses of bis(perfluoroalkyl)phosphinic acid anhydrides.
    这项发明涉及一种通过双(全氟烷基)膦酸与五氧化二磷反应制备双(全氟烷基)膦酸酐的方法,以及新型的双(全氟烷基)膦酸酐和双(全氟烷基)膦酸酐的用途。
  • COMPOUNDS WITH (PERFLUOROALKYL) FLUOROHYDROGENPHOSPHATE ANIONS
    申请人:Ignatyev Nikolai (Mykola)
    公开号:US20120264946A1
    公开(公告)日:2012-10-18
    The present invention relates to a process for the preparation of compounds with (perfluoroalkyl)fluorohydrogenphosphate anion, and to compounds containing (perfluoroalkyl)fluorohydrogenphosphate anion and to the use thereof.
    本发明涉及一种制备含有(全氟烷基)氟氢磷酸盐阴离子的化合物的方法,以及含有(全氟烷基)氟氢磷酸盐阴离子的化合物及其用途。
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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