2-Hydroxy-3,6-dimethylbenzoic acid, also known as salicylic acid derivative, is an aromatic carboxylic acid characterized by the presence of both hydroxyl (-OH) and carboxylic acid (-COOH) functional groups. This compound features a benzene ring substituted with two methyl groups at the 3 and 6 positions and a hydroxyl group at the 2 position, contributing to its acidity and potential for hydrogen bonding. It is typically a white to off-white crystalline solid, exhibiting moderate solubility in water and higher solubility in organic solvents. The presence of the hydroxyl group enhances its reactivity, making it useful in various chemical reactions, including esterification and acylation. This compound may also exhibit biological activity, making it of interest in pharmaceuticals and agrochemicals. Its melting point and boiling point can vary based on purity and environmental conditions. As with many aromatic acids, it may have applications in the synthesis of dyes, fragrances, and as a precursor in organic synthesis. Safety data should be consulted for handling and usage guidelines.

2-hydroxy-3,6-dimethylbenzoic acid

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2-Hydroxy-3,6-dimethylbenzoic acid

2-Hydroxy-3,6-dimethylbenzoic acid is a chromophore that activates enzymes in the biosynthesis of aromatic compounds. It is found in plants and fungi as well as in some bacteria and protists. 2-Hydroxy-3,6-dimethylbenzoic acid has been shown to be a biosynthetic precursor for the production of salicylic acid, an important plant hormone. This compound also plays a role in the biosynthesis of neocarzinostatin, maduropeptin, and other natural products.

CAS 3921-12-8: 2-hydroxy-3,6-dimethylbenzoic acid

2-Hydroxy-3,6-dimethylbenzoic acid

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2-Hydroxy-3,6-dimethylbenzoic acid

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2-Hydroxy-3,6-dimethylbenzoic acid

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