Ethyl 2,6-dihydroxybenzoate, with the CAS number 54640-04-9, is an organic compound that belongs to the class of benzoate esters. It is characterized by the presence of two hydroxyl (-OH) groups located at the 2 and 6 positions of the benzene ring, which contribute to its solubility and reactivity. The ethyl group attached to the carboxylate portion enhances its lipophilicity compared to its parent acid. This compound typically appears as a white to off-white solid or crystalline substance and is soluble in organic solvents such as ethanol and acetone, but less soluble in water due to its hydrophobic ethyl group. Ethyl 2,6-dihydroxybenzoate exhibits antioxidant properties and may be used in various applications, including cosmetics and pharmaceuticals, due to its potential to stabilize formulations. Additionally, its structural features suggest that it may participate in hydrogen bonding, influencing its physical properties and interactions with other molecules. Safety data should be consulted for handling and usage guidelines.

ethyl 2,6-dihydroxybenzoate

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Ethyl 2,6-dihydroxybenzoate is a natural product that can be found in the plant Hypericum perforatum. It has been shown to possess antibacterial and antifungal properties. Ethyl 2,6-dihydroxybenzoate has also been shown to inhibit the activity of phosphatase enzymes and may have use as an anti-inflammatory agent. This compound is synthesized from 3,5-dihydroxybenzoic acid by the enzyme hypericin synthase. The enzyme catalyzes the condensation of two molecules of 3,5-dihydroxybenzoic acid to form ethyl 2,6-dihydroxybenzoate. The reaction requires NADPH as a cofactor and produces one molecule of NADP+ in the process.

CAS 54640-04-9: ethyl 2,6-dihydroxybenzoate

Ethyl 2,6-dihydroxybenzoate

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Ethyl 2,6-dihydroxybenzoate

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Ethyl 2,6-dihydroxybenzoate

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