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Merck

104426

Tetrafluoroterephthalonitrile

99%

Synonym(s):

2,3,5,6-Tetrafluoro-1,4-dicyanobenzene

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About This Item

Linear Formula:
C6F4-1,4-(CN)2
CAS Number:
Molecular Weight:
200.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-397-3
MDL number:
Assay:
99%
Form:
solid
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Product Name

Tetrafluoroterephthalonitrile, 99%

InChI key

PCRSJGWFEMHHEW-UHFFFAOYSA-N

InChI

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

SMILES string

Fc1c(F)c(C#N)c(F)c(F)c1C#N

assay

99%

form

solid

mp

197-199 °C (lit.)

solubility

acetone: soluble

Quality Level

Application

Tetrafluoroterephthalonitrile can be used in the synthesis of Polymers of Intrinsic Microporosity (PIM). Tetrafluoroterephthalonitrile was used to study ultraviolet (UV)-rearranged polymers of PIM-1 membranes for efficient separation of H2 and CO2 .

General description

Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η2-nitrile complexes.

wgk

WGK 3

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Wenmin Zhang et al.
Journal of chromatography. A, 1503, 1-11 (2017-05-14)
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Synthesis and reactivity of tungsten (II) carbonyl ?2-nitrile complexes: crystal structure of tetrafluoroterephthalonitrile as a four-electron donor ligand.
Kiplinger JL, et al.
Chemical Communications (Cambridge, England), 14, 1691-1692 (1996)
Manmatha Mahato et al.
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In the field of bioinspired soft robotics, to accomplish sophisticated tasks in human fingers, electroactive artificial muscles are under development. However, most existing actuators show a lack of high bending displacement and irregular response characteristics under low input voltages. Here
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CO2 cycloaddition to epoxides is an effective and economical utilization method to alleviate the current excessive CO2 emission situation. The development of catalysts with both high catalytic efficiency and high recyclability is necessary but challenging. In this context, a heterogeneous
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Molecular architecture in nanoscale spaces can lead to selective chemical interactions and separation of species with similar sizes and functionality. Substrate specific sorbent chemistry is well known through highly crystalline ordered structures such as zeolites, metal organic frameworks and widely

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