CAS 51116-92-8
:methyl 2-hydroxy-4,6-dimethoxybenzoate
Description:
Methyl 2-hydroxy-4,6-dimethoxybenzoate, with the CAS number 51116-92-8, is an organic compound that belongs to the class of benzoates. It features a benzoic acid derivative structure, characterized by the presence of a methoxy group (-OCH3) at the 4 and 6 positions and a hydroxyl group (-OH) at the 2 position of the aromatic ring. This compound is typically a white to off-white solid and is soluble in organic solvents, reflecting its hydrophobic nature due to the methoxy substituents. Its hydroxyl group contributes to its potential for hydrogen bonding, which can influence its solubility and reactivity. Methyl 2-hydroxy-4,6-dimethoxybenzoate may exhibit biological activity, making it of interest in various fields, including pharmaceuticals and agrochemicals. Additionally, its structure suggests potential applications in organic synthesis and as an intermediate in the production of other chemical compounds. Safety data should be consulted for handling and usage, as with any chemical substance.
Formula:C10H12O5
InChI:InChI=1/C10H12O5/c1-13-6-4-7(11)9(10(12)15-3)8(5-6)14-2/h4-5,11H,1-3H3
SMILES:COc1cc(c(c(c1)OC)C(=O)OC)O
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Found 1 products.
Methyl 4,6-Dimethoxysalicylate
CAS:Controlled Product<p>Applications Methyl 4,6-Dimethoxysalicylate is an intermediate in the synthesis of 2-Hydroxy-4,6-dimethoxybenzoic Acid (H825565). 2-Hydroxy-4,6-dimethoxybenzoic acid is a reagent used in the synthesis of rac Zearalenone-d6 (Z270502). rac Zearalenone-d6 s an estrogenic mycotoxin produced by Fusarium fungi commonly found in grains. One of a group of compounds known as resorcylic acid lactones.<br>References Tanaka, T., et al.: J. Agric. Food Chem., 36, 979 (1988), Hamilton, S., et al.: Anticancer Res., 16, 3597 (1996), Hecht, S., et al.: Cancer Lett., 150, 49 (2000), Hussein, H., et al.: Toxicology, 167, 101 (2001), Lim, H., et al.: J. Immunol., 175, 4180 (2005),<br></p>Formula:C10H12O5Color and Shape:NeatMolecular weight:212.199
