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双[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-十七氟癸基)苯基]苯膦 | 892154-91-5

中文名称
双[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-十七氟癸基)苯基]苯膦
中文别名
双[4-(1H,1H,2H,2H-全氟癸基)苯基]苯基膦
英文名称
bis[4-(1H,1H,2H,2H-perfluoro-7-decyl)phenyl]phenylphospine
英文别名
Bis[4-(1H,1H,2H,2H-perfluorodecyl)phenyl]phenylphosphine;bis[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)phenyl]-phenylphosphane
双[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-十七氟癸基)苯基]苯膦化学式
CAS
892154-91-5
化学式
C38H21F34P
mdl
——
分子量
1154.5
InChiKey
GMHNZJNJORCMQJ-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

  • 熔点:
    65-71 °C

计算性质

  • 辛醇/水分配系数(LogP):
    17.5
  • 重原子数:
    73
  • 可旋转键数:
    21
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    34

安全信息

  • WGK Germany:
    3

SDS

SDS:744a7b3ccf908ddcdba92033f506fbaa
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反应信息

  • 作为反应物:
    描述:
    双[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-十七氟癸基)苯基]苯膦 、 [RuCl2(η6-C6H5(CH2)2CH(OH)CH3)]2 以 氯仿 为溶剂, 以88%的产率得到[Ru(η6-4-phenyl-2-butanol)Cl2(PPh(p-C6H4C2H4C8H17)2)]
    参考文献:
    名称:
    Use of Perfluorinated Phosphines to Provide Thermomorphic Anticancer Complexes for Heat-Based Tumor Targeting
    摘要:
    A series of compounds of general formula [Ru(eta(6)-arene)(pta)(PR3)Cl]BF4 (arene = p-cymene or 4-phenyl-2-butanol; pta = 1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane, PR3 = PPh2(p-C6H4C2H4C8F17), PPh(p-C6H4C2H4C8F17)(2), P(p-C6H4C2H4C6F13)(3), PPh3 or P(p-C6H4F)(3)) have been prepared and characterized by spectroscopic methods. The structure of [Ru(eta(6)-p-cymene)(pta)Cl(P(p-C6H4F)(3))]BF4 has also been established in the solid state by X-ray crystallography. The cytotoxicities of the compounds were determined in the A2780 and A2780 cisplatin-resistant cell lines revealing that the fluorinated phosphines significantly increase antiproliferative activity relative to their bis-chloride precursors. Two of the complexes were found to be thermoresponsive, that is, showing poor water solubility at 37 degrees C and good solubility at 42 degrees C, the temperature of a heated tumor, providing a method of tumor targeting. Incubation at 42 degrees C for 2 h resulted in improved cytotoxicities for two of the complexes.
    DOI:
    10.1021/ic9020433
  • 作为试剂:
    描述:
    N-tert-butoxycarbonyl-2-(2-(methoxymethyloxy)phenyl)-2-oxo-ethylsulfonamideN-甲基磺酰基氨基甲酸叔丁酯双[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-十七氟癸基)苯基]苯膦 、 bis[1H,1H,2H,2H,3H,3H-perfluoro]azodicarboxylate 作用下, 以 四氢呋喃 为溶剂, 反应 12.5h, 以85%的产率得到5'-amino-5'-N,N6-di-tert-butoxycarbonyl-5'-deoxy-2',3'-O-isopropylidene-5'-N-[(2-(2-(methoxymethyloxy)phenyl)-2-oxo-ethyl)sulfonyl]adenosine
    参考文献:
    名称:
    Antibacterial Agents
    摘要:
    这项发明提供了化合物的公式(I)及其盐:R1-L-R2—B,其中R1、L、R2和B具有本文中定义的任何值,以及包含这种化合物的组合物,以及包含这种化合物或盐的治疗方法。这些化合物可以阻断细菌中的铁载体产生,并可用作抗菌剂。
    公开号:
    US20080293666A1
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文献信息

  • Use of Perfluorinated Phosphines to Provide Thermomorphic Anticancer Complexes for Heat-Based Tumor Targeting
    作者:Anna K. Renfrew、Rosario Scopelliti、Paul J. Dyson
    DOI:10.1021/ic9020433
    日期:2010.3.1
    A series of compounds of general formula [Ru(eta(6)-arene)(pta)(PR3)Cl]BF4 (arene = p-cymene or 4-phenyl-2-butanol; pta = 1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane, PR3 = PPh2(p-C6H4C2H4C8F17), PPh(p-C6H4C2H4C8F17)(2), P(p-C6H4C2H4C6F13)(3), PPh3 or P(p-C6H4F)(3)) have been prepared and characterized by spectroscopic methods. The structure of [Ru(eta(6)-p-cymene)(pta)Cl(P(p-C6H4F)(3))]BF4 has also been established in the solid state by X-ray crystallography. The cytotoxicities of the compounds were determined in the A2780 and A2780 cisplatin-resistant cell lines revealing that the fluorinated phosphines significantly increase antiproliferative activity relative to their bis-chloride precursors. Two of the complexes were found to be thermoresponsive, that is, showing poor water solubility at 37 degrees C and good solubility at 42 degrees C, the temperature of a heated tumor, providing a method of tumor targeting. Incubation at 42 degrees C for 2 h resulted in improved cytotoxicities for two of the complexes.
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