83766-52-3 (4-全氟辛基苯胺,4-Perfluorooctylaniline)

CAS号:
83766-52-3
中文名称:
4-全氟辛基苯胺
英文名称:
4-Perfluorooctylaniline
安全信息:
分子式:
C14H6F17N
分子量:
511.177003383636

4-全氟辛基苯胺(83766-52-3)名称与标识符

名称

中文别名:
4-全氟辛基苯胺;4-(十七氟辛基)苯胺;
英文别名:
4-Perfluorooctylaniline;4-(Heptadecafluorooctyl)aniline;4-(Perfluorooctyl)aniline;4-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Heptadecafluorooctyl)benzenamine (ACI);Benzenamine, 4-(heptadecafluorooctyl)- (9CI);4-(Perfluorooctyl)benzenamine;p-Heptadecafluorooctylaniline;DTXSID10392660;NS00109160;ZQTZVMUNYIDMJV-UHFFFAOYSA-N;MFCD28134623;4-(Heptadecafluorooctyl)aniline, >=95.0% (GC);83766-52-3;4-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl)aniline;SCHEMBL486692;G79342;

标识符

MDL:
MFCD28134623
InChIKey:
ZQTZVMUNYIDMJV-UHFFFAOYSA-N
Inchi:
1S/C14H6F17N/c15-7(16,5-1-3-6(32)4-2-5)8(17,18)9(19,20)10(21,22)11(23,24)12(25,26)13(27,28)14(29,30)31/h1-4H,32H2
SMILES:
FC(C(C(C(C(C(C(C(C1C=CC(N)=CC=1)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F

4-全氟辛基苯胺(83766-52-3)物化性质

实验特性

  • 折射率 : 1.359
  • 沸点 : 272.1 °C at 760 mmHg
  • 熔点 : 42-47 °C
  • 闪点 : 272.1 °C at 760 mmHg
  • 颜色与性状 : 无色晶体
  • 溶解性 : 未确定
  • 密度 : 1.61

计算特性

  • 精确分子量 : 511.023
  • 氢键供体数量 : 1
  • 氢键受体数量 : 1
  • 可旋转化学键数量 : 8
  • 同位素质量 : 511.023
  • 重原子数量 : 32
  • 复杂度 : 671
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 6.8
  • 互变异构体数量 : 无
  • 表面电荷 : 0
  • 拓扑分子极性表面积 : 26A^2

4-全氟辛基苯胺(83766-52-3)合成路线

合成路线:1 步
参考文献:
Syntheses of azobenzene derivatives having fluoroalkyl chain and their monomolecular film formation at the air/water interface
Yoshino, Norio; et al, Bulletin of the Chemical Society of Japan, 1992, 65(8), 2141-4
合成路线:1 步
反应条件:
参考文献:
Synthesis and catalytic activity of fluorous chiral primary amine-thioureas
Orlandi, Simonetta; et al, New Journal of Chemistry, 2013, 37(12), 4140-4147
合成路线:1 步
反应条件:
参考文献:
Synthesis and characterization of photoresponsive POSS-based polymers and their switchable water and oil wettability on cotton fabric
Huang, Jianbao; et al, RSC Advances, 2015, 5(121), 100339-100346
合成路线:1 步
参考文献:
Direct perfluoroalkylation of functionalized benzenes with perfluoroalkyl halides and copper bronze
Fuchikami, Takamasa; et al, Journal of Fluorine Chemistry, 1983, 22(6), 541-56
合成路线:1 步
反应条件:
参考文献:
Highly Site-Selective Formation of Perfluoroalkylated Anilides via a Protecting Strategy by Molybdenum Hexacarbonyl Catalyst
Yuan, Chunchen; et al, Organic Letters, 2019, 21(16), 6481-6484
合成路线:2 步
反应条件:
参考文献:
Highly Site-Selective Formation of Perfluoroalkylated Anilides via a Protecting Strategy by Molybdenum Hexacarbonyl Catalyst
Yuan, Chunchen; et al, Organic Letters, 2019, 21(16), 6481-6484
合成路线:1 步
反应条件:
参考文献:
Benign Perfluoroalkylation of Aniline Derivatives through Photoredox Organocatalysis under Visible-Light Irradiation
Barata-Vallejo, Sebastian; et al, European Journal of Organic Chemistry, 2015, 2015(36), 7869-7875
合成路线:1 步
反应条件:
参考文献:
Benign Perfluoroalkylation of Aniline Derivatives through Photoredox Organocatalysis under Visible-Light Irradiation
Barata-Vallejo, Sebastian; et al, European Journal of Organic Chemistry, 2015, 2015(36), 7869-7875