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111331-32-9

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111331-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111331-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,3,3 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111331-32:
(8*1)+(7*1)+(6*1)+(5*3)+(4*3)+(3*1)+(2*3)+(1*2)=59
59 % 10 = 9
So 111331-32-9 is a valid CAS Registry Number.

111331-32-9Downstream Products

111331-32-9Relevant academic research and scientific papers

Skeletal transformations and fluorination of perfluoroalkylbenzenes in reactions with antimony pentafluoride

Karpov,Mezhenkova,Platonov

, p. 1176 - 1181 (2007/10/03)

Reaction of octafluorotoluene and perfluoro-m-xylene with tetrafluoroethylene in the presence of SbF5 yielded perfluorinated propyl-and 1,3-dipropylbenzene, and propyltoluene. The perfluoropropyl group of these compounds under the action of SbF5 at 200°C is transformed into perfluoroisopropyl or trifluoromethyl group. Polyfluoroalkylbenzenes in SbF5 medium undergo fluorinationb to afford perfluoro1-alkylcyclohexenes.

FLUORINATION OF POLYHALOGENATED UNSATURATED COMPOUNDS WITH VANADIUM PENTAFLUORIDE

Bardin, V. V.,Avramenko, A. A.,Furin, G. G.,Krasilnikov, V. A.,Karelin, A. I.,et al.

, p. 385 - 400 (2007/10/02)

Vanadium pentafluoride reacts with polyfluorinated and polychlorinated olefins, alkadienes, cycloalkenes and cyclodienes in CFCl3 or without a solvent at -25 deg C to 100 deg C, forming products of addition of two fluorine atoms across the C=C bond.

REACTION OF POLYHALOGENATED UNSATURATED COMPOUNDS WITH VANADIUM PENTAFLUORIDE

Petrov, V. A.,Bardin, V. V.,Furin, G. G.,Avramenko, A. A.,Galakhov, M. V.,et al.

, p. 37 - 41 (2007/10/02)

Terminal polyhalogenoalkenes are fluorinated by vanadium pentafluoride at -20 to -30 deg C, whereas internal polyfluoroalkenes only react with vanadium pentafluoride when heated. 2-Chloropentafluoro-1,3-butadiene adds fluorine atoms predominantly at positions 1,4 under the influence of vanadium pentafluoride, but only the isomeric tetrafluorohexachlorobutanes are formed from perchloro-1,3-butadiene.Fluorination of perfluoroallylbenzene and perfluoro-β-methylstyrene takes place more rapidly in the side chain than in the aromatic ring.

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