Methyl 3,5-dihydroxy-4-iodo-benzoate, identified by its CAS number 338454-02-7, is an organic compound that belongs to the class of benzoate esters. This substance features a benzoic acid derivative with hydroxyl groups at the 3 and 5 positions and an iodine atom at the 4 position of the aromatic ring. The presence of these functional groups contributes to its chemical reactivity and potential biological activity. The hydroxyl groups can participate in hydrogen bonding, influencing the compound's solubility and interaction with other molecules. As an ester, it may undergo hydrolysis in the presence of water, leading to the release of the corresponding alcohol and acid. The iodine substituent can impart unique properties, such as increased lipophilicity and potential applications in medicinal chemistry. Overall, methyl 3,5-dihydroxy-4-iodo-benzoate is of interest in various fields, including pharmaceuticals and agrochemicals, due to its structural characteristics and potential biological effects.

methyl 3,5-dihydroxy-4-iodo-benzoate

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Methyl 3,5-dihydroxy-4-iodobenzoate is a natural product that was discovered in a soil sample from the Philippines. It is an isobenzofuranone that can be synthesized by coupling two geranyl acetates and methylating the hydroxyl group. This compound has not been found to have any known biological activity. Methyl 3,5-dihydroxy-4-iodobenzoate is synthesized by reacting acetic anhydride with methyl iodide and sodium hydroxide in methanol. The yields for this synthesis are about 50%.

CAS 338454-02-7: methyl 3,5-dihydroxy-4-iodo-benzoate

Methyl 3,5-dihydroxy-4-iodobenzoate

Ref: 3D-NNA45402

Methyl 3,5-dihydroxy-4-iodobenzoate

Ref: 54-OR93709

Methyl 3,5-dihydroxy-4-iodobenzoate

Ref: 10-F339794

methyl 3,5-dihydroxy-4-iodobenzoate

Ref: IN-DA00CL1R