Behrman, E. J. et al. published their research in Organic Reactions (Hoboken, NJ, United States) in 1988 | CAS: 52010-89-6

2,5-Dihydroxy-4-methylbenzaldehyde (cas: 52010-89-6) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Synthetic Route of C8H8O3

The persulfate oxidation of phenols and arylamines (the Elbs and the Boyland-Sims oxidations) was written by Behrman, E. J.. And the article was included in Organic Reactions (Hoboken, NJ, United States) in 1988.Synthetic Route of C8H8O3 The following contents are mentioned in the article:

A review of the article The persulfate oxidation of phenols and arylamines (the Elbs and the Boyland-Sims oxidations). This study involved multiple reactions and reactants, such as 2,5-Dihydroxy-4-methylbenzaldehyde (cas: 52010-89-6Synthetic Route of C8H8O3).

2,5-Dihydroxy-4-methylbenzaldehyde (cas: 52010-89-6) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Synthetic Route of C8H8O3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts