248061
Octafluoronaphthalene
96%
Synonym(s):
1,2,3,4,5,6,7,8-Octafluoronaphthalene, Perfluoronaphthalene
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1 G
€49.70
About This Item
Empirical Formula (Hill Notation):
C10F8
CAS Number:
Molecular Weight:
272.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
96%
form
solid
mp
87-88 °C (lit.)
functional group
fluoro
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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.
Takanori Iwasaki et al.
Chemistry, an Asian journal, 15(8), 1349-1354 (2020-02-28)
Changes in the photophysical properties of pyrene (Py)-octafluoronaphthalene (OFN) co-crystals (Py⋅OFN) upon mechanical stimuli are described herein. The Py⋅OFN co-crystal showed a mechano-induced bathochromic shift in emission, and a similar tendency was observed for the 1,3,6,8-tetramethylpyrene-OFN co-crystal. These shifts are
A phase transformation with no change in space group symmetry; octafluoronaphthalene.
Pawley GS and Dietrich O-W.
Journal of Physics C: Solid State Physics, 8(16), 2549-2549 (1975)
Yohanna Alegre et al.
Food research international (Ottawa, Ont.), 122, 1-9 (2019-06-24)
Polyfunctional mercaptans are powerful wine aroma compounds formed from cysteinylated and glutathionylated precursors present in grapes. The concentration of polyfunctional mercaptans in the wines is not directly correlated to the concentration of their precursors in the juices, which suggests that
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