196819
Tetrafluorophthalonitrile
95%
Synonym(s):
1,2-Dicyano-3,4,5,6-tetrafluorobenzene, 3,4,5,6-Tetrafluoro-1,2-benzenedicarbonitrile
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About This Item
Linear Formula:
C6F4(CN)2
CAS Number:
Molecular Weight:
200.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-400-8
MDL number:
Assay:
95%
InChI key
OFLRJMBSWDXSPG-UHFFFAOYSA-N
InChI
1S/C8F4N2/c9-5-3(1-13)4(2-14)6(10)8(12)7(5)11
SMILES string
Fc1c(F)c(F)c(C#N)c(C#N)c1F
assay
95%
mp
81-86 °C (lit.)
functional group
fluoro, nitrile
Quality Level
General description
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
Application
Tetrafluorophthalonitrile was used in the synthesis of dichloro-subphthalocyanine dimers.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Polyfluoroarenes. Part XI. Reactions of tetrafluorophthalonitrile with nucleophilic reagents.
Birchall JM, et al.
J. Chem. Soc. Sect. C, 3, 456-462 (1970)
The synthesis of highly fluorinated phthalonitrile resins and cure studies.
Keller TM and Griffith JR.
Journal of Fluorine Chemistry, 13(4), 315-324 (1979)
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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