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bis(pentafluoroethyl)phosphinic acid chloride | 103304-95-6

中文名称
——
中文别名
——
英文名称
bis(pentafluoroethyl)phosphinic acid chloride
英文别名
bis(pentafluoroethyl)phosphinyl chloride;1-[chloro(1,1,2,2,2-pentafluoroethyl)phosphoryl]-1,1,2,2,2-pentafluoroethane
bis(pentafluoroethyl)phosphinic acid chloride化学式
CAS
103304-95-6
化学式
C4ClF10OP
mdl
——
分子量
320.454
InChiKey
ICIJWVXTJKISHG-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:
    135.0±40.0 °C(Predicted)
  • 密度:
    1.734±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 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:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    11

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 chloride 作用下, 以 乙醚 为溶剂, 反应 0.58h, 以58%的产率得到bis(pentafluoroethyl)phosphinyl amide
    参考文献:
    名称:
    WO2006/128563
    摘要:
    公开号:
  • 作为产物:
    参考文献:
    名称:
    氯双(五氟乙基)膦:气相中改进的合成和分子结构
    摘要:
    (C 2 F 5)2 PC1现在可以通过从技术产品(C 2 F 5)3 PF 2开始的显着改进的合成方案访问。(C 2 F 5)3 PF 2的第一步是在120°C的无溶剂反应中用NaBH 4还原。用过量的氢氧化钠水溶液处理产物P(C 2 F 5)3,得到相应的次膦酸盐Na +(C 2 F 5)2PO -选择下五氟乙烷的解放。随后用PhPCl 4氯化导致(C 2 F 5)2 PCl选择性形成,通过分步冷凝将其分离,总产率为66%。(C 2 F 5)2的气体电子衍射(GED)图记录了PC1,并发现它由两个一致性模型进行描述。对势能表面的量子化学研究表明,可能存在许多低能构象体,每个构象体都有许多低频振动模式,因此具有大振幅运动。通过GED还发现,计算出的最稳定的构象异构体最丰富,占总数的61(5)%。通过GED测定的分子结构参数与在理论上在MP2 / TZVPP水平上计算的参数相吻合。唯一的显
    DOI:
    10.1002/chem.201003048
  • 作为试剂:
    描述:
    bis(pentafluoroethyl)phosphinic acid四氯苯基-膦烷bis(pentafluoroethyl)phosphinic acid chloride 作用下, 反应 4.0h, 以giving 18.1 g of bis(pentafluoroethyl)phosphinyl chloride, which的产率得到bis(pentafluoroethyl)phosphinic acid chloride
    参考文献:
    名称:
    Method for producing bis(fluoralkyl)phosphinic acid chlorides or fluoralkylphosphonic acid chlorides
    摘要:
    本发明涉及一种制备双(氟烷基)膦酰氯或氟烷基膦酸二氯化物的方法,通过将相应的双(氟烷基)膦酸或氟烷基膦酸与芳基四氯化膦作为氯化剂反应。
    公开号:
    US08378157B2
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文献信息

  • [EN] PHOSPHINYL HYDRAZIDES<br/>[FR] HYDRAZIDES DE PHOSPHINYLE
    申请人:MERCK PATENT GMBH
    公开号:WO2011095277A1
    公开(公告)日:2011-08-11
    This invention relates to fluorinated phosphinyl hydrazides, a process for their preparation, and the use of these compounds, especially in organic synthesis.
    这项发明涉及氟代磷酰肼,其制备方法,以及这些化合物的用途,特别是在有机合成中的应用。
  • Synthesis and Characterization of New BIS(Pentafluoroethyl)Phosphinic Acid Amides and Hydrazides. Crystal Structure of (C<sub>2</sub>F<sub>5</sub>)<sub>2</sub>P(O)NH<sub>2</sub>
    作者:Dana Bejan、Vasile Dinoiu、Nikolai Ignat’ev、Eduard Bernhardt、Helge Willner
    DOI:10.1080/10426507.2013.865127
    日期:2014.10.3
    GRAPHICAL ABSTRACT Abstract Previously unknown bis(pentafluoroethyl)phosphinyl amides and hydrazides have been prepared in good yields by the reaction of bis(pentafluoroethyl)phosphinyl chloride or tris(pentafluoroethyl)phosphine oxide with the corresponding primary amines or hydrazines. The crystal structure of (C2F5)2P(O)NH2 was determined. The compound (C2F5)2P(O)NH-NHCH2C6H2-3,5-(t-C4H9)-4-OH was oxidized
    图形摘要摘要通过双(五氟乙基)膦酰氯或三(五氟乙基)氧化膦与相应的伯胺或肼反应,已经以良好的收率制备了以前未知的双(五氟乙基)膦酰酰胺和酰肼。确定了(C2F5)2P(O)NH2 的晶体结构。化合物 (C2F5)2P(O)NH-NHCH2C6H2-3,5-(t-C4H9)-4-OH 用 PbO2 氧化成相应的氧自由基。
  • Bis(perfluoralkyl)phosphinous acids and derivatives and use thereof
    申请人:Hoge Berthold
    公开号:US20110124873A1
    公开(公告)日:2011-05-26
    The invention relates to bis(perfluoroalkyl)phosphinous acids, bis(perfluoroalkyl)thiophosphinous acids and derivatives, the synthesis thereof and the use thereof, in particular for the synthesis of air-stable metal complexes for catalytic processes.
    这项发明涉及双(全氟烷基)膦酸、双(全氟烷基)硫膦酸及其衍生物,其合成和用途,特别是用于合成用于催化过程的空气稳定金属配合物。
  • 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。
  • METHOD FOR PRODUCING BIS(FLUORALKYL)PHOSPHINIC ACID CHLORIDES OR FLUORALKYLPHOSPHONIC ACID CHLORIDES
    申请人:Ignatyev Nikolai(Mykola)
    公开号:US20110124921A1
    公开(公告)日:2011-05-26
    The invention relates to a process for the preparation of bis(fluoroalkyl)phosphinyl chlorides or fluoroalkylphosphonyl dichlorides by reaction of the corresponding bis(fluoroalkyl)phosphinic acid or fluoroalkylphosphonic acid with aryltetrachlorophosphorane as chlorinating agent
    该发明涉及一种通过将相应的双(氟烷基)膦酸或氟烷基膦酸与芳基四氯膦作为氯化剂反应,制备双(氟烷基)膦酰氯或氟烷基膦酰二氯化物的方法。
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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