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MilliporeSigma

248061

Sigma-Aldrich

Octafluoronaphthalene

96%

Sinónimos:

1,2,3,4,5,6,7,8-Octafluoronaphthalene, Perfluoronaphthalene

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About This Item

Fórmula empírica (notación de Hill):
C10F8
Número de CAS:
Peso molecular:
272.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

96%

form

solid

mp

87-88 °C (lit.)

SMILES string

Fc1c(F)c(F)c2c(F)c(F)c(F)c(F)c2c1F

InChI

1S/C10F8/c11-3-1-2(5(13)9(17)7(3)15)6(14)10(18)8(16)4(1)12

InChI key

JDCMOHAFGDQQJX-UHFFFAOYSA-N

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Polycyclic fluoroaromatic compounds. Part XII.[1] The extent of 1-substitution in octafluoronaphthalene.
Burdon J and Rimmington TW.
Journal of Fluorine Chemistry, 27(3), 257-261 (1985)
Qimeng Jiang et al.
Polymers, 12(7) (2020-07-28)
Solid acid catalysts generally show the disadvantage of low acid amount and low recycling rate. To solve these problems, corn stalk-based solid acid catalysts were synthesized through carbonization and sulfonation processes in this work. The results showed that besides the
J C Collings et al.
Acta crystallographica. Section C, Crystal structure communications, 57(Pt 7), 870-872 (2001-07-10)
The structure of the title complex, C10F8*C14H10, comprises mixed stacks of alternating diphenylacetylene and octafluoronaphthalene molecules, both lying at inversion centres and parallel to within 8.6 (1) degrees, in contrast with the herring-bone packing observed in crystals of either pure
Amination of octafluoronaphthalene in liquid ammonia: 2, 6-and 2, 7-Diaminohexafluoronaphthalenes selective preparation.
Journal of Fluorine Chemistry, 129(4), 253-260 (2008)
Roque Serrano et al.
Analytical and bioanalytical chemistry, 413(4), 1039-1046 (2020-11-20)
The characterization of very long-chain (>C24) polyunsaturated fatty acids (VLC-PUFAs), which are essential in the vision, neural function, and reproduction of vertebrates, is challenging because of the lack of reference standards and their very low concentrations in certain lipid classes.

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