815-23-6 Usage
General Description
Bromopentafluoroacetone is a specialty chemical most commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals, such as pesticides. Characterized by five fluorine atoms and a bromine atom attached to a ketone functional group in its molecular structure, it holds unique reactivity and stability properties. It is also appreciated for its resistance to high temperatures and strong acids, which makes it relevant in industries that require stringent chemical conditions. Nonetheless, due to the high reactivity of bromines, it requires careful handling and storage to avoid hazards, especially because it can produce toxic fumes if heated or coming into contact with other reactive chemicals. As with many brominated and fluorinated compounds, its environmental and health effects are closely monitored due to potential toxicity and ozone depletion concerns.
Check Digit Verification of cas no
The CAS Registry Mumber 815-23-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 815-23:
(5*8)+(4*1)+(3*5)+(2*2)+(1*3)=66
66 % 10 = 6
So 815-23-6 is a valid CAS Registry Number.
InChI:InChI=1/C3BrF5O/c4-2(5,6)1(10)3(7,8)9
815-23-6Relevant articles and documents
Interaction of perfluorinated α-fluorosulfatocarbonyl compounds with nucleophilic reagents
Delyagina, N. I.,Avetisyan, E. A.,Rogovik, V. M.,Cherstkov, V. F.,Sterlin, S. R.,German, L. S.
, p. 217 - 222 (1993)
α-Perfluorosulfatoperfluorocarbonyl compounds interact with alkaline metals halogenides to form the corresponding α-halo derivatives as a result of the direct nucleophilic substitution of the FSO3 group.Through the action of halogenide anions on perfluorinated α,β-bis-fluorosulfatocarbonyl compounds, substitution by halogen of the FSO3 group in the α-position to the carbonyl takes place.However, the FSO3 group in the β-position is cleaved, which allows α-substituted β-dicarbonyl derivatives to be obtained.
REDUCTIVE DEFLUORINATION OF HEXAFLUOROACETONE AND THE SYNTHESIS OF HALOPENTAFLUOROACETONES
Postovoi, S. A.,Vol'pin, I. M.,Mysov, E. I.,Zeifman, Yu. V.,German, L. S.
, p. 1067 - 1070 (2007/10/02)
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