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N-phenyl perfluorooctanesulfonamide | 559-05-7

中文名称
——
中文别名
——
英文名称
N-phenyl perfluorooctanesulfonamide
英文别名
heptadecafluoro-octane-1-sulfonic acid anilide;Heptadecafluor-octan-1-sulfonsaeure-anilid;1-Octanesulfonamide, 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-N-phenyl-;1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-N-phenyloctane-1-sulfonamide
N-phenyl perfluorooctanesulfonamide化学式
CAS
559-05-7
化学式
C14H6F17NO2S
mdl
——
分子量
575.246
InChiKey
URBBAHQFHYXVEH-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:
    317.4±52.0 °C(Predicted)
  • 密度:
    1.699±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.7
  • 重原子数:
    35
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    54.6
  • 氢给体数:
    1
  • 氢受体数:
    20

SDS

SDS:72c7a4d2b7801551f3f7e4e53ab31cbe
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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

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文献信息

  • 512. Perfluoroalkyl derivatives of sulphur. Part VI. Perfluoroalkanesulphonic acids CF<sub>3</sub>·[CF<sub>2</sub>]<sub>n</sub>·SO<sub>3</sub>H (n= 1—7)
    作者:T. Gramstad、R. N. Haszeldine
    DOI:10.1039/jr9570002640
    日期:——
  • Synthesis and surface activities of organic solvent-soluble fluorinated surfactants
    作者:Guo-Li Li、Li-Qiang Zheng、Jin-Xin Xiao
    DOI:10.1016/j.jfluchem.2009.05.006
    日期:2009.7
    A variety of fluorinated surfactants soluble in organic solvent were prepared, including C8F17SO2NHCnH2n+1 (n = 2, 4, 6, 8, 10), C8F17SO2NHR (R = C6H11, C6H5), C8F17SO2N(C(n)H(2)n(+1))(2) (n = 1, 2, 3, 4) and C8F17SO2NH(CH2)(n)NHO2SC8F17 (n = 6, 10). Their surface activities in various organic solvents were determined by surface tension measurement. The results showed that these fluorinated surfactants can reduce the surface tension of both polar and non-polar organic solvents. In general, organic solvents with strong polarity or long alkyl chain are beneficial to increase the surface activity of these polar fluorinated surfactants. By comparing fluorinated surfactants with the same fluorocarbon segment and connecting group, C8F17SO2N(CnH2n+1)(2) (n = 1, 2, 3, 4) showed lower surface activity in organic solvents than C8F17SO2NHCnH2n+1 (n = 2, 4, 6, 8) with an equal carbon number of the solvophilic group. Through surface tension vs. concentration curves given for N-octyl perfluorooctanesulfonamide in various organic solvents, a break point like the critical micelle concentration of ordinary surfactants in aqueous solutions was observed, and the effect of the different types of organic solvents on adsorption and aggregation behavior was also studied. (C) 2009 Elsevier B.V. All rights reserved.
  • Burdon, J.; Farazmand, I.; Stacey, M., Journal of the Chemical Society
    作者:Burdon, J.、Farazmand, I.、Stacey, M.、Tatlow, J. C.
    DOI:——
    日期:——
  • Burdon et al., Journal of the Chemical Society, 1957, p. 2574,2576
    作者:Burdon et al.
    DOI:——
    日期:——
  • JPH07331009A
    申请人:——
    公开号:JPH07331009A
    公开(公告)日:1995-12-19
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