Deady, Leslie W. et al. published their research in Australian Journal of Chemistry in 1983 | CAS: 24103-75-1

4-Methoxy-2-methylpyridine (cas: 24103-75-1) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Pyridine groups exist in countless molecules, and their applications include catalysis, drug design, molecular recognition, and natural product synthesis.HPLC of Formula: 24103-75-1

Catalysis by α-substituted pyridines in the hydrolysis of aryl acetates and acetic anhydride was written by Deady, Leslie W.;Finlayson, Wayne L.. And the article was included in Australian Journal of Chemistry in 1983.HPLC of Formula: 24103-75-1 This article mentions the following:

Rate constants for the hydrolyses of p-nitrophenyl acetate (I), 2,4-dinitrophenyl acetate (II) and, acetic anhydride in the presence of α-substituted pyridines were determined Broensted LFER plots for I and II were linear over 4 pKa units. The 2-Me and 2-NH2 substituted pyridines catalyze the hydrolyses by a nucleophilic mechanism. In the experiment, the researchers used many compounds, for example, 4-Methoxy-2-methylpyridine (cas: 24103-75-1HPLC of Formula: 24103-75-1).

4-Methoxy-2-methylpyridine (cas: 24103-75-1) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Pyridine groups exist in countless molecules, and their applications include catalysis, drug design, molecular recognition, and natural product synthesis.HPLC of Formula: 24103-75-1

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem