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perfluoro(5-aza-4-nonene) | 148123-76-6

中文名称
——
中文别名
——
英文名称
perfluoro(5-aza-4-nonene)
英文别名
perfluoro(5-azanon-4-ene);perfluoro-5-aza-4-nonene;Per-fluoro-5-azanon-4-ene;(1Z)-2,2,3,3,4,4,4-heptafluoro-N-(1,1,2,2,3,3,4,4,4-nonafluorobutyl)butanimidoyl fluoride
perfluoro(5-aza-4-nonene)化学式
CAS
148123-76-6
化学式
C8F17N
mdl
——
分子量
433.068
InChiKey
DVQXCHAOWHNHSQ-CYPCERQJSA-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:
    86.8±50.0 °C(Predicted)
  • 密度:
    1.71±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    12.4
  • 氢给体数:
    0
  • 氢受体数:
    18

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    全氟(5-氮杂-4-壬烯)与肼及其衍生物的反应
    摘要:
    The reaction of perfluoro(5-aza-4-nonene) with hydrazine hydrate in tetrahydrofuran at 0-20degreesC in the presence of triethylamine yields 2,5-bis(heptafluoropropyl)-1H-1,2,4-triazole; under similar conditions perfluoro(5-aza-4-nonene) reacts with arylhydrazines to form 1-aryl-3,5-bis(heptafluoropropyl)-1,2,4-triazoles.
    DOI:
    10.1023/a:1013876707892
  • 作为产物:
    描述:
    perfluoro(di-n-butylmethylamine)五氟化锑 作用下, 反应 3.0h, 以92%的产率得到perfluoro(5-aza-4-nonene)
    参考文献:
    名称:
    Cleavage of perfluorinated tertiary amines by antimony pentafluoride
    摘要:
    DOI:
    10.1007/bf00953712
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文献信息

  • Oxyfunctionalization reactions by perfluoro cis-2,3-dialkyloxaziridines. Enantioselective conversion of silanes into silanols
    作者:Marcello Cavicchioli、Vittorio Montanari、Giuseppe Resnati
    DOI:10.1016/s0040-4039(00)73424-1
    日期:1994.8
    Perfluoro cis-2,3-dialkyloxaziridine 2 is shown to perform the oxyfunctionalization of silanes 1 under very mild conditions to give silanols and silanediols 3 in high chemical yields and complete enantioselectivity.
    显示全氟顺式2,3-二烷基恶唑烷2在非常温和的条件下进行硅烷1的氧官能化,从而以高化学产率和完全对映选择性得到硅烷醇和硅烷二醇3。
  • Synthesis of Heterocyclic Compounds Containing Perfluoroalkyl Groups. Reactions of Perfluoro(2-methyl-2-pentene) and Perfluoro(5-aza-4-nonene) with N,S-Dinucleophiles
    作者:G. G. Furin、E. L. Zhuzhgov
    DOI:10.1007/s11178-005-0183-1
    日期:2005.3
    Perfluoro(2-methyl-2-pentene) and perfluoro(5-aza-4-nonene) react with 1,4,5,6-tetrahydropyrimi-dine-2-thiol, pyridine-2-thiol, and 1,2,4-triazole-3-thiol to afford fused heterocyclic systems, while their reactions with tetrahydrothiazole-2-thione and pyrimidine-2-thiol result in replacement of the fluorine atom at the double bond. Treatment of 3,3,3-trifluoro-1-pentafluoroethyl-2-trifluoromethyl-1-pentenyl isothiocyanate with ammonia gives N-(3,3,3-trifluoro-1-pentafluoroethyl-2-trifluoromethyl-1-propenyl)thiourea which undergoes ring closure to 4-tetrafluoroethylidene-5,5-bis(trifluoromethyl)-4,5-dihydrothiazol-2-amine. Possible cyclization paths and the effect of the 1,3(N,S)-dinucleophile nature on the direction of nucleophilic addition at the double bond are discussed.
    全氟(2-甲基-2-戊烯)和全氟(5-氮-4-壬烯)与1,4,5,6-四氢嘧啶-2-硫醇、吡啶-2-硫醇和1,2,4-三唑-3-硫醇反应,生成融合的杂环系统,而它们与四氢噻唑-2-硫酮和嘧啶-2-硫醇的反应则导致双键处氟原子的取代。将3,3,3-三氟-1-五氟乙基-2-三氟甲基-1-烯基异硫氰酸酯与氨反应可得到N-(3,3,3-三氟-1-五氟乙基-2-三氟甲基-1-丙烯基)硫脲,该化合物经过环化形成4-四氟乙烯基-5,5-双(三氟甲基)-4,5-二氢噻唑-2-胺。讨论了可能的环化路径及1,3(N,S)-二亲核试剂的性质对双键处亲核加成方向的影响。
  • Efficient interconversion of α,α-difluoromethylenephosphonates and α,α-difluoromethylenephosphonothioates
    作者:Serge R. Piettre
    DOI:10.1016/0040-4039(96)00912-4
    日期:1996.7
    Treatment of dialkyl 1,1-difluoromethylenephosphonates 1 with Lawesson's reagent cleanly produces the corresponding dialkyl 1,1-difluoromethylenephosphonothioates 2. The reaction can be extended to dialkyl 1,1-difluoromethylenephosphinates and to dialkyl 1,1-difluoromethylenephosphine oxides. The reversed transformation (i.e. converting dialkyl 1,1-difluoromethylenephosphonothioates into dialkyl 1
    用Lawesson试剂处理二烷基1,1-二氟亚甲基膦酸酯1可以干净地产生相应的二烷基1,1-二氟亚甲基膦硫酸酯2。该反应可以扩展为1,1-二氟亚甲基次膦酸二烷基酯和1,1-二氟亚甲基次膦氧化物二烷基。反转变换(即转换的二烷基1,1- difluoromethylenephosphonothioates成二烷基1,1- difluoromethylenephosphonates)是最方便地通过使用双环氧乙烷达到7或全氟-顺式-2- Ñ丁基-3- Ñ -propyloxaziridine 8,并产生所希望的高产率的膦酸酯。讨论了这些转换的综合兴趣。
  • Stable odorant systems
    申请人:Loughnane Joseph Brian
    公开号:US20070123440A1
    公开(公告)日:2007-05-31
    This invention relates to stable odorant systems, compositions comprising such systems and processes for making and using such systems and compositions.
    本发明涉及稳定的香味剂系统、包含此类系统的组合物、制备和使用此类系统和组合物的方法。
  • Composition comprising a lipase and a bleach catalyst
    申请人:Souter Philip Frank
    公开号:US20070173429A1
    公开(公告)日:2007-07-26
    The present invention relates to a composition comprising: (i) a lipase; and (ii) a bleach catalyst that is capable of accepting an oxygen atom from a peroxyacid and transferring the oxygen atom to an oxidizeable substrate.
    本发明涉及一种组合物,其包括:(i)一种脂肪酶;和(ii)一种漂白剂催化剂,该催化剂能够从过氧酸中接受一个氧原子,并将该氧原子转移给可氧化底物。
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同类化合物

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