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双(三氟甲基)过氧化物 | 927-84-4

中文名称
双(三氟甲基)过氧化物
中文别名
——
英文名称
bis(trifluoromethyl)peroxide
英文别名
Bis(trifluoromethyl) peroxide;trifluoro(trifluoromethylperoxy)methane
双(三氟甲基)过氧化物化学式
CAS
927-84-4
化学式
C2F6O2
mdl
MFCD00042072
分子量
170.011
InChiKey
BPXRXDJNYFWRDI-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    8

安全信息

  • 海关编码:
    2909600000

SDS

SDS:87f3b301f87104d3622321157a2f924a
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反应信息

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文献信息

  • Perfluoroalkyl derivatives of nitrogen. Part XXV. The reactions of tristrifluoromethylhydroxylamine and mercuric bistrifluoromethylamide with unsaturated systems
    作者:R. N. Haszeldine、A. E. Tipping
    DOI:10.1039/j39670001241
    日期:——
    obutane), and lower yields of other products including perfluoro-(1,2-bisdimethylaminocyclobutane), perfluoro-(2,2′-dimethoxybicyclobutyl), and perfluoro-(2-dimethylamino-2′-methoxybicyclobutyl). Reaction with perfluorobut-2-ene is more complex. Perfluoro-2-azapropene gives low yields of the two isomeric 1:1 adducts perfluoro-(2,3-dimethyl-5-oxa-2,3-diazahexane) and perfluoro-(3,5-dimethyl-2-oxa-3
    三氟甲基羟胺在辐照下与全氟环丁烯反应,生成全氟-(1-二甲基氨基-2-甲氧基环丁烷)1:1加合物,并降低其他产物的收率,包括全氟-(1,2-双二甲基氨基环丁烷),全氟-(2,2 '-二甲氧基双环丁基)和全氟-(2-二甲基氨基-2'-甲氧基双环丁基)。与全氟丁-2-烯的反应更为复杂。全氟-2-氮杂丙烯使全氟-(2,3-二甲基-5-氧杂-2,3-二氮杂己烷)和全氟-(3,5-二甲基-2-氧杂-3)的两种异构体1:1加合物的收率低,5-重氮己烷)。
  • From hypochlorites to perfluorinated dialkyl peroxides
    作者:Jan H. Nissen、Lucas Wickemeyer、Tony Stüker、Simon Steinhauer、Helmut Beckers、Sebastian Riedel
    DOI:10.1016/j.jfluchem.2019.109416
    日期:2020.2
    The synthesis and characterization of the new perfluorinated hypochlorite, undecafluoro-tert-pentyl hypochlorite, (C2F5)(F3C)2COCl, is reported. Its gas-phase infrared, UV/Vis and NMR spectra have been recorded and its spectroscopic properties are discussed and compared with quantum-chemical predictions and those of other known perfluorinated hypochlorites such as RFOCl [RF = F3C, (F3C)3C, (C2F5)(F3C)2C]
    据报道,新的全氟化次氯酸盐,十氟叔丁基戊基次氯酸盐(C 2 F 5)(F 3 C)2 COCl的合成和表征。已记录了其气相红外,UV / Vis和NMR光谱,并讨论了其光谱性质,并将其与量子化学预测以及其他已知的全氟化次氯酸盐如R F OCl [R F = F 3 C,(F 3 C)3 C,(C 2 F 5)(F 3 C)2C]。相应的次氯酸盐的低温光解也提供了合成途径,以其他方式难以获得的全氟化二烷基过氧化物R F OOR F。
  • The conversion of perfluoro-olefins, perfluoroketones or perfluoroacids into perfluoroethers, perfluoroalkylperoxides or perfluorocarbons
    作者:R.N. Haszeldine
    DOI:10.1016/s0022-1139(00)83241-8
    日期:1985.8
    Part of a study to synthesise via radical reactions perfluoroalkanes containing oxygen is illustrated with the olefin (CF3)2C:C(CF3)2. Photochemical oxidation of the olefin with short reaction time gives the ketones CF3.CO.CF(CF3)2 (48% yield), CF3.O.CF2.CO.CF3, CF3.O.CF2.CO.CF(CF3)2 and CF3.CO.CF3. The epoxide is a by-product not an intermediate in these reactions.
    通过自由基反应合成含氧的全氟烷烃的部分研究用烯烃(CF 3)2 C:C(CF 3)2进行说明。用短的反应时间对烯烃进行光化学氧化,得到酮CF 3 .CO.CF(CF 3)2(48%收率),CF 3 .CF。CF 2 .CO.CF 3,CF 3 .O.CF 2。 CO.CF(CF 3)2和CF 3 .CO.CF 3。环氧化物是这些反应中的副产物而不是中间体。
  • Comparative studies of the catalytic fluorination of carbon monoxide with elementary fluorine
    作者:Manfred Wechsberg、George H. Cady
    DOI:10.1021/ja01044a019
    日期:1969.7
    Abstract : AgF2 is a catalyst for the reaction, CO + F2 = CF2O and for subsequent changes in which COF2 reacts with fluorine to give CF3OF and CF3OOCF3. Cesium fluoride aids in the production of CF3OF but not CF3OOCF3 from fluorine and COF2. (Author)
    摘要 : AgF2 是反应的催化剂,CO + F2 = CF2O 以及 COF2 与氟反应生成 CF3OF 和 CF3OOCF3 的后续变化。氟化铯有助于从氟和 COF2 生产 CF3OF,但不有助于生产 CF3OOCF3。(作者)
  • 7-(or 6-) Substituted-7-(or 6-)acylimino cephalosporin (or penicillin)
    申请人:Merck & Co., Inc.
    公开号:US04296236A1
    公开(公告)日:1981-10-20
    A process is provided which yields derivatives of cephalosporins and penicillins. The process starts with 7-aminodecephalosporanic acid or 6-APA and reacts with a carbonyl containing compound to form a Schiff's base (imino) adduct. This latter compound is then treated with a defined reactant yielding a novel Schiff's base adduct having a side chain on the carbon adjacent to the imino-nitrogen. The amino moiety can be regenerated and further reacted to form end compounds which are active against both gram-positive and gram-negative bacteria.
    提供了一种制备头孢菌素和青霉素衍生物的方法。该方法从7-氨基头孢菌烷酸或6-APA开始,与含有羰基的化合物反应,形成席夫碱(亚胺)加合物。然后,用一种定义的反应剂处理这种化合物,得到一种新的席夫碱加合物,其侧链位于亚胺-氮的相邻碳上。氨基基团可以再生并进一步反应,形成对革兰氏阳性和阴性细菌都具有活性的最终化合物。
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