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α-Methylbenzyl anion, also known as α-methylbenzyl carbanion, is a chemical species with the molecular formula C8H9-. It is formed by the deprotonation of α-methyltoluene, where a hydrogen atom is removed from the benzylic position, resulting in a negatively charged carbon atom. This anion is resonance-stabilized, with the negative charge delocalized over the aromatic ring, making it a relatively stable carbanion. α-Methylbenzyl anion plays a significant role in various organic reactions, such as nucleophilic aromatic substitution and carbon-carbon bond formation, due to its strong nucleophilic character. Its stability and reactivity make it an important intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

13822-53-2

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13822-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13822-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13822-53:
(7*1)+(6*3)+(5*8)+(4*2)+(3*2)+(2*5)+(1*3)=92
92 % 10 = 2
So 13822-53-2 is a valid CAS Registry Number.

13822-53-2Upstream product

13822-53-2Downstream Products

13822-53-2Relevant academic research and scientific papers

On the Generation and Characterization of the Spirooctadienyl Anion in the Gas Phase

Maas, Wilfrid P. M.,Veelen, Peter A. van,Nibbering, Nico M. M.

, p. 546 - 558 (1989)

Three routes have been explored in both a high-pressure chemical ionization (CI) source and a low-pressure Fourier transform ion cyclotron resonance (FT-ICR) cell to generate the spirooctadienyl anion in the gas phase: (i) proton abstraction from spiroocta-4,6-diene; (ii) expulsion of trimethylsilyl fluoride by phenyl ring participation following fluoride anion attack upon the silicon centre of 2-phenylethyl trimethylsilane; and (iii) collisionally induced dissociation (CID) of the carboxylate anion of 3-phenylpropanoic acid via carbon dioxide loss.From comparison of the CID spectra of various reference (1-) ions with those of the (1-) ions with those of the (1-) ions which could be generated via the routes (i) and (iii) in the CI source it can be concluded that only the third route yields a (1-) in whose CID spectrum is not inconsistent with the one expected for the spirooctadienyl anion.In the FT-ICR cell (1-) ions are generated along all three routes; their structures have been identified by specific ion-molecule reactions and appear to be different.Route (i) yields an α-methyl benzyl anion, probably due to isomerization within the ion-molecule complex formed.An ortho-ethylphenyl anions is formed along route (ii), presumably due to an intramolecular ortho proton abstraction in the generated trimethylsilyl fluoride solvated 2-phenylethyl primary carbanion.The (1-) ion formed along route (iii) shows reactions similar to those of the 1,1-dimethylcyclohexadienyl anion which is structurally related to the spirooctadienyl anion.Furthermore, the (1-) ion generated via route (iii) reacts with hexafluorobenzene under expulsion of only one hydrogen fluoride molecule which contains exclusively one of the original phenyl ring hydrogen atoms.On the basis of all these observations it is therefore quite likely that the spirooctadienyl anion is formed by collisionally induced decarboxylation of the 3-phenylpropanoic acid carboxylate anion and can be a long-lived and stable species in the gas phase.

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