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N-Methylperfluoro-p-toluidine | 28012-06-8

中文名称
——
中文别名
——
英文名称
N-Methylperfluoro-p-toluidine
英文别名
N-methyl-perfluoro-4-toluidine;2,3,5,6-tetrafluoro-N-methyl-4-(trifluoromethyl)aniline
N-Methylperfluoro-p-toluidine化学式
CAS
28012-06-8
化学式
C8H4F7N
mdl
——
分子量
247.115
InChiKey
PETXUCXQNAUQRK-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:
    177.3±40.0 °C(Predicted)
  • 密度:
    1.551±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    8

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-Methylperfluoro-p-toluidine盐酸 、 sodium nitrite 作用下, 反应 2.0h, 以94%的产率得到N-Nitroso-N-methylperfluoro-p-toluidine
    参考文献:
    名称:
    Polyfluorinated arylnitrosamines
    摘要:
    N-Methyl-, N-n-butyl-, N-t-butylperfluoroarylamines undergo nitrosation with nitrous acid to give the corresponding N-nitroso derivatives. Perfluoroaryl groups were selected from the benzene, indane, biphenyl, naphthalene and pyridine series. According to H-1 and F-19 NMR spectra, N-nitroso-N-methyl derivatives of polyfluoroarenes, consist of E and Z isomers with the former prevailing. The more bulky n-butyl group promotes an increase in the formation of Z isomers. Only Z isomers have been obtained from N-t-butyl derivatives of perfluorinated 4-toluidine and 4-aminopyridine. The structure of the Z isomer of N-nitroso-N-methylperfluoro-4-toluidine is confirmed by X-ray data. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-1139(01)00567-x
  • 作为产物:
    描述:
    八氟甲苯甲胺异丙醇 为溶剂, 反应 72.0h, 以96%的产率得到N-Methylperfluoro-p-toluidine
    参考文献:
    名称:
    Polyfluorinated arylnitramines
    摘要:
    N-methyl- and N-butylperfluoroarylamines are transformed by HNO3 into N-nitro-N-methyl- and N-nitro-N-butylperfluoroarylamines. These reactions were used to synthesise N-nitro-N-methylpentafluoroaniline and its p-CF3. -CN, -C6F5 substituted derivatives, N-nitro-N-methylperfluoro-2,4-xylidine, N-nitro-N-methyl-4-aminotetrafluoropyridine N-nitro-N-methyl 5-aminoperfluoroindane, N-nitro-N-methyl-2- aminoheptafluoronaphthalene. 4,4 ' -bis(N-nitro-N- merhylamino)octafluorobiphenyl from 4,4 ' -bis(N-methylamino)octafluorobiphenyl, N-nitro-N-n-butylpentafluoroaniline, N-nitro-N-n-butylperfluoro-p-toluidine, N-nitro-N-n-butyl-4-aminotetrafluoropyridine and N-nitro-bis( perfluoro-p-tolyl)amine. Tetrafluoro-p-benzoquinone and heptafluoro-p-toluquinol were obtained from N-methylpentafluoroanilinz and N-methylperfluoro-p-toluidine, respectively, under the action of a mixture of HNO3 and H2SO4 The X-ray crystal structure of N-nitro-N-methylperfluoro-p-toluidine was determined. (C) 2001 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-1139(01)00367-0
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文献信息

  • Kobrina,L.S. et al., Journal of Organic Chemistry USSR (English Translation), 1970, vol. 6, p. 510 - 517
    作者:Kobrina,L.S. et al.
    DOI:——
    日期:——
  • RADECK, WOLFGANG;PLATONOV, VJACHESLAV E.;POPKOVA, NINA V.
    作者:RADECK, WOLFGANG、PLATONOV, VJACHESLAV E.、POPKOVA, NINA V.
    DOI:——
    日期:——
  • [EN] POLYMERIC ORGANIC NANOPARTICLES WITH ENHANCED EMISSION<br/>[FR] NANOPARTICULES ORGANIQUES POLYMÈRES À ÉMISSION AMÉLIORÉE
    申请人:SONY CORP
    公开号:WO2017167631A1
    公开(公告)日:2017-10-05
    The present disclosure relates to luminescent including photon up-conversion nanoparticles. These nanoparticles include a polymeric organic matrix, at least one light emitter distributed within this matrix, a stabilizing agent, and at least one metal particle enclosed within the matrix, wherein the metal particles are plasmonic nanoparticles. The present disclosure further relates to methods of manufacture and to uses of such nanoparticles.
  • Polyfluorinated arylnitramines
    作者:V.E Platonov、A Haas、M Schelvis、M Lieb、K.V Dvornikova、O.I Osina、Yu.V Gatilov
    DOI:10.1016/s0022-1139(01)00367-0
    日期:2001.7
    N-methyl- and N-butylperfluoroarylamines are transformed by HNO3 into N-nitro-N-methyl- and N-nitro-N-butylperfluoroarylamines. These reactions were used to synthesise N-nitro-N-methylpentafluoroaniline and its p-CF3. -CN, -C6F5 substituted derivatives, N-nitro-N-methylperfluoro-2,4-xylidine, N-nitro-N-methyl-4-aminotetrafluoropyridine N-nitro-N-methyl 5-aminoperfluoroindane, N-nitro-N-methyl-2- aminoheptafluoronaphthalene. 4,4 ' -bis(N-nitro-N- merhylamino)octafluorobiphenyl from 4,4 ' -bis(N-methylamino)octafluorobiphenyl, N-nitro-N-n-butylpentafluoroaniline, N-nitro-N-n-butylperfluoro-p-toluidine, N-nitro-N-n-butyl-4-aminotetrafluoropyridine and N-nitro-bis( perfluoro-p-tolyl)amine. Tetrafluoro-p-benzoquinone and heptafluoro-p-toluquinol were obtained from N-methylpentafluoroanilinz and N-methylperfluoro-p-toluidine, respectively, under the action of a mixture of HNO3 and H2SO4 The X-ray crystal structure of N-nitro-N-methylperfluoro-p-toluidine was determined. (C) 2001 Elsevier Science B.V. All rights reserved.
  • Polyfluorinated arylnitrosamines
    作者:Vyacheslav E. Platonov、Alois Haas、Meinolf Schelvis、Max Lieb、Kira V. Dvornikova、Olga I. Osina、Tatyana V. Rybalova、Yuri V. Gatilov
    DOI:10.1016/s0022-1139(01)00567-x
    日期:2002.3
    N-Methyl-, N-n-butyl-, N-t-butylperfluoroarylamines undergo nitrosation with nitrous acid to give the corresponding N-nitroso derivatives. Perfluoroaryl groups were selected from the benzene, indane, biphenyl, naphthalene and pyridine series. According to H-1 and F-19 NMR spectra, N-nitroso-N-methyl derivatives of polyfluoroarenes, consist of E and Z isomers with the former prevailing. The more bulky n-butyl group promotes an increase in the formation of Z isomers. Only Z isomers have been obtained from N-t-butyl derivatives of perfluorinated 4-toluidine and 4-aminopyridine. The structure of the Z isomer of N-nitroso-N-methylperfluoro-4-toluidine is confirmed by X-ray data. (C) 2002 Elsevier Science B.V. All rights reserved.
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