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bis(heptafluoropropyl)phenylphosphine | 20608-39-3

中文名称
——
中文别名
——
英文名称
bis(heptafluoropropyl)phenylphosphine
英文别名
Bis(heptafluoropropyl)(phenyl)phosphane;bis(1,1,2,2,3,3,3-heptafluoropropyl)-phenylphosphane
bis(heptafluoropropyl)phenylphosphine化学式
CAS
20608-39-3
化学式
C12H5F14P
mdl
——
分子量
446.123
InChiKey
BUFRJKRCCDDRQO-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:
    198.8±40.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.6
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    14

SDS

SDS:d03e717133ab8d29eac104f31cac7a5e
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反应信息

  • 作为反应物:
    描述:
    bis(heptafluoropropyl)phenylphosphine盐酸氢氧化钾甲酸 作用下, 以 二氯甲烷 为溶剂, 反应 5.0h, 生成 苯膦酸
    参考文献:
    名称:
    Yagupol'skii, L. M.; Pavlenko, N. V.; Ignat'ev, N. V., Journal of general chemistry of the USSR, 1984, vol. 54, # 2, p. 297 - 302
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    叔烷基(全氟烷基)膦的制备和水解
    摘要:
    膦R(R F)2 P(R F = CF 3,R = Me,Bu n,Bu i,Ph; R F = C 3 F 7,R = Bu n,Ph)和Bu 2 n(CF 3)P和亚氯氯化物Bu(CF 3)PCl,是由氯化物(R F)2 PCl或R F PCl 2和有机锂化合物在–78°的乙醚-己烷溶液中制得的。膦R 2(C 3 F 7)P(R = Et,Ph,CF 3)和CF 3(C 3 F 7)2 P已经由化合物R 2 PCl或CF 3 PCl 2和七氟丙基-锂制得。将膦(CF 3)2(C 3 F 7)P用二氧化氮氧化为氧化膦(CF 3)2(C 3 F 7)PO,将其用水水解。讨论了红外光谱和核磁共振光谱。化合物R(CF 3)2的水解在水-乙醇中带有碱的P遵循第二级动力学,并且在25°时的速率常数按R = Bu n > Bu i > Ph的顺序降低。CF 3比C 3 F 7更容易从不对称膦(CF 3)2(C
    DOI:
    10.1039/j19680001909
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文献信息

  • Yagupol'skii, L. M.; Popov, V. I.; Pavlenko, N. V., Journal of Organic Chemistry USSR (English Translation), 1986, vol. 22, # 10, p. 1947 - 1950
    作者:Yagupol'skii, L. M.、Popov, V. I.、Pavlenko, N. V.、Maletina, I. I.、Mironova, A. A.、et al.
    DOI:——
    日期:——
  • YAGUPOLSKIJ, L. M.;PAVLENKO, N. V.;IGNATEV, N. V.;MATYUSHECHEVA, G. I.;SE+, ZH. OBSHCH. XIMII, 1984, 54, N 2, 334-339
    作者:YAGUPOLSKIJ, L. M.、PAVLENKO, N. V.、IGNATEV, N. V.、MATYUSHECHEVA, G. I.、SE+
    DOI:——
    日期:——
  • YAGUPOLSKIJ L. M.; POPOV V. I.; PAVLENKO N. V.; MALETINA I. I.; MIRONOVA +, ZH. ORGAN. XIMII, 22,(1986) N 10, 2169-2173
    作者:YAGUPOLSKIJ L. M.、 POPOV V. I.、 PAVLENKO N. V.、 MALETINA I. I.、 MIRONOVA +
    DOI:——
    日期:——
  • Yagupol'skii, L. M.; Pavlenko, N. V.; Ignat'ev, N. V., Journal of general chemistry of the USSR, 1984, vol. 54, # 2, p. 297 - 302
    作者:Yagupol'skii, L. M.、Pavlenko, N. V.、Ignat'ev, N. V.、Matyushecheva, G. I.、Semenii, V. Ya.
    DOI:——
    日期:——
  • The preparation and hydrolysis of tertiary alkyl(perfluoroalkyl)phosphines
    作者:K. Gosling、D. J. Holman、J. D. Smith、B. N. Ghose
    DOI:10.1039/j19680001909
    日期:——
    The phosphines R(RF)2P (RF= CF3, R = Me, Bun, Bui, Ph; RF= C3F7, R = Bun, Ph) and Bu2n(CF3)P, and the phosphinous chloride Bu(CF3)PCl, have been made from the chlorides (RF)2PCl or RFPCl2 and organolithium compounds in ether–hexane at –78°. The phosphines R2(C3F7)P (R = Et, Ph, CF3) and CF3(C3F7)2P have been made from the compounds R2PCl or CF3PCl2 and heptafluoropropyl-lithium. The phosphine (CF3)2(C3F7)P
    膦R(R F)2 P(R F = CF 3,R = Me,Bu n,Bu i,Ph; R F = C 3 F 7,R = Bu n,Ph)和Bu 2 n(CF 3)P和亚氯氯化物Bu(CF 3)PCl,是由氯化物(R F)2 PCl或R F PCl 2和有机锂化合物在–78°的乙醚-己烷溶液中制得的。膦R 2(C 3 F 7)P(R = Et,Ph,CF 3)和CF 3(C 3 F 7)2 P已经由化合物R 2 PCl或CF 3 PCl 2和七氟丙基-锂制得。将膦(CF 3)2(C 3 F 7)P用二氧化氮氧化为氧化膦(CF 3)2(C 3 F 7)PO,将其用水水解。讨论了红外光谱和核磁共振光谱。化合物R(CF 3)2的水解在水-乙醇中带有碱的P遵循第二级动力学,并且在25°时的速率常数按R = Bu n > Bu i > Ph的顺序降低。CF 3比C 3 F 7更容易从不对称膦(CF 3)2(C
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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