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α-Trifluoracetophenon-radikalanion, also known as α-trifluoromethylphenacyl radical anion, is a chemical species derived from α-trifluoromethylphenacyl bromide, a synthetic precursor. This radical anion is characterized by the presence of a delocalized π-radical system, which is stabilized by the electron-withdrawing trifluoromethyl group. It plays a significant role in various chemical reactions, particularly in the context of radical-mediated processes and organic synthesis. The α-trifluoracetophenon-radikalanion is of interest to chemists due to its unique electronic properties and potential applications in the development of new synthetic methods and materials.

20813-35-8

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20813-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20813-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20813-35:
(7*2)+(6*0)+(5*8)+(4*1)+(3*3)+(2*3)+(1*5)=78
78 % 10 = 8
So 20813-35-8 is a valid CAS Registry Number.

20813-35-8Downstream Products

20813-35-8Relevant academic research and scientific papers

Electron transfer as a possible initial step in nucleophilic addition elimination reactions between (radical) anions and carbonyl compounds in the gas phase

Staneke, Paul O.,Ingemann, Steen,Nibbering, Nico M. M.

, p. 179 - 184 (2007/10/03)

The reactions of the HO-, CH3S-, CH2S- and CH2=C(CH3)-CH2- ions with three ketones (CF3COR; R=CH3, CF3, C6H5) and three esters of trifluoroacetic acid (CF3CO2R; R=CH3, C2H5 and C6H5) have been studied with use of Fourier Transform Ion Cyclotron Resonance (FT-ICR) mass spectrometry. All four negative ions react exclusively by proton transfer with CF3COCH3. With the other substrates, the HO- ion reacts by various pathways, such as proton transfer, SN2 substitution, E2 elimination and attack on the carbonyl group. The CH3S- ion is unreactive towards CF3COC6H5 but is able to react by hydride transfer, SN2, E2 and/or carbonyl attack with the remaining neutral species. The CH2S- radical anion reacts by electron transfer to afford stable molecular radical anions of CF3COCF3 and CF3COC6H5, whereas the main reaction with the two esters, CF3CO2CH3 and CF3CO2C2H5, is dissociative electron transfer leading to CF3CO2- and CF3- ions. The CH2=C(CH3)-CH2- anion displays a more complex reactivity pattern involving electron transfer, SN2, E2 as well as attack on the carbonyl group. Direct evidence for the occurrence of electron transfer as the initial step in an overall BAC2 type process has not been obtained for the systems studied. The reaction of the CH2S- ion with CF3CO2C6H5 was observed, however, to yield exclusively a CF3COCHS-. radical anion. Based upon the absence of a BAC2 process in the reaction of CH2S- with the methyl and ethyl esters of trifluoroacetic acid in combination with the facile occurrence of electron transfer from this radical anion, it is suggested that the CF3COCHS-. ion is formed by an initial electron transfer followed by coupling between the CH2S molecule and the CF3CO2C6H5- radical anion and subsequent loss of C6H5OH from the collision complex.

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