248061
Octafluoronaphthalene
96%
Synonym(s):
1,2,3,4,5,6,7,8-Octafluoronaphthalene, Perfluoronaphthalene
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About This Item
Empirical Formula (Hill Notation):
C10F8
CAS Number:
Molecular Weight:
272.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
206-239-9
MDL number:
Product Name
Octafluoronaphthalene, 96%
InChI key
JDCMOHAFGDQQJX-UHFFFAOYSA-N
InChI
1S/C10F8/c11-3-1-2(5(13)9(17)7(3)15)6(14)10(18)8(16)4(1)12
SMILES string
Fc1c(F)c(F)c2c(F)c(F)c(F)c(F)c2c1F
assay
96%
form
solid
mp
87-88 °C (lit.)
functional group
fluoro
Quality Level
signalword
Warning
hcodes
Hazard Classifications
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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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
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
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.
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)
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