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1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate

中文名称
——
中文别名
——
英文名称
1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate
英文别名
[MMIM][(C2F5)2P(O)O];1,3-Dimethylimidazolium bis(pentafluoroethyl)phosphinate;bis(1,1,2,2,2-pentafluoroethyl)phosphinate;1,3-dimethylimidazol-1-ium
1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate化学式
CAS
——
化学式
C4F10O2P*C5H9N2
mdl
——
分子量
398.14
InChiKey
DOTLTWIBLXONEK-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):
    2.78
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    48.9
  • 氢给体数:
    0
  • 氢受体数:
    12

反应信息

  • 作为产物:
    描述:
    N-甲基咪唑methyl ester of bis(pentafluoroethyl)phosphinic acid 以96%的产率得到1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate
    参考文献:
    名称:
    PROCESS FOR THE PREPARATION OF PHOSPHINIC ACID ESTERS
    摘要:
    该发明涉及一种通过将相应的膦氧化物与醇或酚在碱金属氟化物或四烷基铵氟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。
    公开号:
    US20150045572A1
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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:US09056881B2
    公开(公告)日:2015-06-16
    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.
    本发明涉及一种制备烷基磷酸酯、烯基磷酸酯、炔基磷酸酯或苯基磷酸酯的方法,通过在碱化物或四烷基化物的存在下,将相应的膦氧化物与醇或反应。
  • Electrochemical deblocking solution for electrochemical oligomer synthesis on an electrode array
    申请人:CustomArray, Inc.
    公开号:US10006131B1
    公开(公告)日:2018-06-26
    There is disclosed an electrochemical deblocking solution for use on an electrode microarray. There is further disclosed a method for electrochemical synthesis on an electrode array using the electrochemical deblocking solution. The solution and method are for removing acid-labile protecting groups for synthesis of oligonucleotides, peptides, small molecules, or polymers on a microarray of electrodes while substantially improving isolation of deblocking to active electrodes. The method comprises applying a voltage or a current to at least one electrode of an array of electrodes. The array of electrodes is covered by the electrochemical deblocking solution.
    本发明公开了一种用于电极微阵列的电化学解锁溶液。还进一步公开了一种使用该电化学解锁溶液在电极阵列上进行电化学合成的方法。该溶液和方法用于去除酸性保护基团,以便在电极微阵列上合成寡核苷酸、肽、小分子或聚合物,同时大幅提高与活性电极的解锁隔离度。该方法包括向电极阵列中的至少一个电极施加电压或电流。电极阵列被电化学解锁溶液覆盖。
  • High efficiency, small volume nucleic acid synthesis
    申请人:LIFE TECHNOLOGIES CORPORATION
    公开号:US10407676B2
    公开(公告)日:2019-09-10
    The disclosure generally relates to compositions and methods for the production of nucleic acid molecules. In some aspects, the invention allows for the microscale generation of nucleic acid molecules, optionally followed by assembly of these nucleic acid molecules into larger molecules. In some aspects, the invention allows for efficient production of nucleic acid molecules (e.g., large nucleic acid molecules such as genomes).
    本发明一般涉及生产核酸分子的组合物和方法。在某些方面,本发明可以微量生成核酸分子,然后将这些核酸分子组装成更大的分子。在某些方面,本发明可高效生产核酸分子(如基因组等大核酸分子)。
  • ELECTROCHEMICAL DEBLOCKING USING A HYDRAZINE DERIVATIVE
    申请人:Combimatrix Corporation
    公开号:EP1805206A2
    公开(公告)日:2007-07-11
  • ELECTROCHEMICAL DEBLOCKING SOLUTION FOR ELECTROCHEMICAL OLIGOMER SYNTHESIS ON AN ELECTRODE ARRAY
    申请人:Combimatrix Corporation
    公开号:EP1869061A2
    公开(公告)日:2007-12-26
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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