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3-pentadecafluoroheptyl-5-pentafluorophenyl-1,2,4-oxadiazole | 919489-99-9

中文名称
——
中文别名
——
英文名称
3-pentadecafluoroheptyl-5-pentafluorophenyl-1,2,4-oxadiazole
英文别名
3-(Pentadecafluoroheptyl)-5-(pentafluorophenyl)-1,2,4-oxadiazole;3-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,7-pentadecafluoroheptyl)-5-(2,3,4,5,6-pentafluorophenyl)-1,2,4-oxadiazole
3-pentadecafluoroheptyl-5-pentafluorophenyl-1,2,4-oxadiazole化学式
CAS
919489-99-9
化学式
C15F20N2O
mdl
——
分子量
604.146
InChiKey
YROHNOYMVCOFGS-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:
    298.7±50.0 °C(Predicted)
  • 密度:
    1.760±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.2
  • 重原子数:
    38
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    38.9
  • 氢给体数:
    0
  • 氢受体数:
    23

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis of fluorinated first generation starburst molecules containing a triethanolamine core and 1,2,4-oxadiazoles
    作者:Silvestre Buscemi、Andrea Pace、Antonio Palumbo Piccionello、Nicolò Vivona
    DOI:10.1016/j.jfluchem.2006.07.012
    日期:2006.12
    functionalize the aliphatic primary hydroxyl functionalities of triethanolamine, under mild conditions. UV–visible absorption and emission spectra are reported, for both tri- and difunctionalised molecules, showing their potential applications as light-emitters in optoelectronic devices.
    合成了5-五氟苯基-1,2,4-恶二唑在C(3)处不同的位置,并在温和条件下用于官能化三乙醇胺的脂肪族伯羟基官能团。报告了三官能和双官能分子的紫外可见吸收光谱和发射光谱,显示了它们在光电器件中作为发光体的潜在应用。
  • Synthesis of a fluorinated graphene oxide–silica nanohybrid: improving oxygen affinity
    作者:A. Maio、D. Giallombardo、R. Scaffaro、A. Palumbo Piccionello、I. Pibiri
    DOI:10.1039/c6ra02585d
    日期:——
    modified method, the GO–silica nanohybrid (GOS) was obtained via Fischer esterification, the fluorinated moiety (3-pentadecafluoroheptyl-5-perfluorophenyl-1,2,4-oxadiazole) was introduced by nucleophilic substitution operated by the hydroxyl functionalities onto the GOS surface. Full characterization of the new materials confirmed the formation of covalent bonds between the graphene oxide/silica hybrid
    提出了一种简便的方法来实现化氧化石墨烯-二氧化硅纳米杂化物(GOSF)。用Hummer改进的方法合成了氧化石墨烯(GO)。费歇尔酯化反应中,通过羟基官能团操作的亲核取代作用将化部分(3-十五庚基-5-全氟苯基-1,2,4-恶二唑)引入GOS表面。新材料的全面表征证实了氧化石墨烯/二氧化硅杂化基质与化部分之间形成了共价键。所提出的方法提供了一种获得化碳/二氧化硅杂化纳米材料的简便方法,从而避免了通常在制备化材料时所涉及的苛刻反应条件,并允许选择性固定特定的尾。此外,进行的氧气吸收和释放动力学表明,化部分的引入增加了氧的交换,
  • Fluorinated and pegylated polyaspartamide derivatives to increase solubility and efficacy of Flutamide
    作者:Antonio Palumbo Piccionello、Giovanna Pitarresi、Andrea Pace、Daniela Triolo、Pasquale Picone、Silvestre Buscemi、Gaetano Giammona
    DOI:10.3109/1061186x.2012.680961
    日期:2012.6
    New fluorinated amphiphilic copolymers based on a biocompatible polyaspartamide have been prepared in order to obtain polymeric micelles useful for delivering anticancer drugs. In particular, alpha,beta-poly(N-2-hydroxyethyl)-(D), (L)-aspartamide (PHEA) has been derivatized with polyethylene glycol (PEG(2000)) and ethylendiamine (EDA). Both these portions form the hydrophilic part of the copolymer, while the hydrophobic moiety is given by 1,2,4-oxadiazoles: 5-pentafluorophenyl-3-perfluoroheptyl-1,2,4-oxadiazole (PPOX) or 3-carboxyethyl-5-pentadecafluoroheptyl-1,2,4oxadiazole (CPOX). Copolymers named PHEA-PEG(2000)-EDA-PPOX and PHEA-PEG(2000)-EDA-CPOX have been prepared with various degrees of derivatization and characterized by spectroscopic analyses. Size exclusion chromatography, pyrene colorimetric assay, light scattering analysis and scanning electron microscopy have evidenced the occurrence of a self-association process in aqueous medium. The ability of these aggregates to incorporate a hydrophobic drug and increase its solubility has been evaluated by using Flutamide, a fluorinated anticancer agent. Moreover, the activity of Flutamide-loaded micelles on proliferation of dihydrotestosterone stimulated LNCaP cells has been determined and compared to that of free drug.
  • Lower rim arylation of calix[n]arenes with extended perfluorinated domains
    作者:Silvestre Buscemi、Andrea Pace、Antonio Palumbo Piccionello、Sebastiano Pappalardo、Domenico Garozzo、Tullio Pilati、Giuseppe Gattuso、Andrea Pappalardo、Ilenia Pisagatti、Melchiorre F. Parisi
    DOI:10.1016/j.tetlet.2006.10.092
    日期:2006.12
    Exhaustive O-arylation of p-tert-butylcalix[n]arenes 2 (n = 4-8) with an excess of 3-pentadecafluoroheptyl-5-pentafluorophenyl-1,2,4-oxadiazole 3 and K2CO3 in refluxing acetonitrile provides an easy entry to a new family of perfluorinated calix[n]arenes 1. The cyclic tetramer furnishes a mixture of cone, partial cone, and 1,2-alternate conformers, while the larger macrocycles afford single products. The structures of all new compounds are substantiated by NMR techniques and MALDI-TOF mass spectral data. Single-crystal X-ray diffraction studies on the pentamer derivative 1b reveal a distorted cone-in conformation of the calixarene cup. (c) 2006 Elsevier Ltd. All rights reserved.
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