196819

Sigma-Aldrich

Tetrafluorophthalonitrile

95%

Sinônimo(s):
3,4,5,6-Tetrafluoro-1,2-benzenedicarbonitrile, 1,2-Dicyano-3,4,5,6-tetrafluorobenzene
Fórmula linear:
C6F4(CN)2
Número CAS:
Peso molecular:
200.09
Número EC:
Número MDL:
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

100

teor

95%

pf

81-86 °C (lit.)

SMILES string

Fc1c(F)c(F)c(C#N)c(C#N)c1F

InChI

1S/C8F4N2/c9-5-3(1-13)4(2-14)6(10)8(12)7(5)11

InChI key

OFLRJMBSWDXSPG-UHFFFAOYSA-N

Descrição geral

Tetrafluorophthalonitrile reacts with:
  • copper, copper (I) chloride or copper (II) chloride to yield copper (II) hexadecafluorophthalocyanine
  • potassium salt of 2-hydroxyhexafluoro-2-propylbenzene to yield 2-phenyl-2-(3,4-dicyano- trifluorophenoxy) hexafluoropropane
  • dipotassium salt of 1,3-bis(2-hdroxyhexafluoro-2- propyl) benzene to yield fluorinated phthalonitrile resins

Aplicação

Tetrafluorophthalonitrile was used in the synthesis of dichloro-subphthalocyanine dimers.

Embalagem

1 g in glass bottle

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Órgãos-alvo

Respiratory system

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

RIDADR

NONH for all modes of transport

WGK Alemanha

WGK 3

Ponto de fulgor (ºF)

Not applicable

Ponto de fulgor (ºC)

Not applicable

The synthesis of highly fluorinated phthalonitrile resins and cure studies.
Keller TM and Griffith JR.
Journal of Fluorine Chemistry, 13(4), 315-324 (1979)
Polyfluoroarenes. Part XI. Reactions of tetrafluorophthalonitrile with nucleophilic reagents.
Birchall JM, et al.
J. Chem. Soc. Sect. C, 3, 456-462 (1970)
Synthesis, separation, and characterization of the topoisomers of fused bicyclic subphthalocyanine dimers.
Christian G Claessens et al.
Angewandte Chemie (International ed. in English), 41(14), 2561-2565 (2002-08-31)
Thi Hai Quyen Nguyen et al.
Physical chemistry chemical physics : PCCP, 22(15), 7699-7709 (2020-03-07)
The transport of both electrons and ions in organic mixed ionic and electronic conductors such as phthalocyanines, is essential to allow redox reactions of entire films and, hence, to impart electrochromism. Thin films of a new type, tetrakis-perfluoroisopropyl-perfluoro phthalocyanine, F40PcCu...
Dongkun Yu et al.
The journal of physical chemistry. B, 123(23), 4958-4966 (2019-05-24)
The concept of eutectic molecular liquids (EMLs) was defined, and a strategy to form EMLs based on noncovalent interactions was proposed. We verified the formation and investigated the properties, interaction sites, and interaction energies of the obtained 16 EMLs. Moreover...

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