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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%
Quality Level
assay
95%
mp
81-86 °C (lit.)
functional group
fluoro, nitrile
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
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 196819-1G | 04061838762238 |
