CAS 5427-29-2

methyl 4-(benzyloxy)-2-hydroxybenzoate

Description:

Methyl 4-(benzyloxy)-2-hydroxybenzoate, with the CAS number 5427-29-2, is an organic compound that belongs to the class of benzoates. It features a methyl ester functional group, a hydroxy group, and a benzyloxy substituent on a benzene ring, which contributes to its chemical properties. This compound is typically characterized by its aromatic structure, which enhances its stability and reactivity. It is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals or agrochemicals. The presence of the hydroxy group suggests potential for hydrogen bonding, which can influence its solubility and interaction with other molecules. Additionally, the benzyloxy group can provide steric hindrance, affecting the compound's reactivity. Methyl 4-(benzyloxy)-2-hydroxybenzoate may exhibit moderate to low solubility in water, while being more soluble in organic solvents, making it useful in various chemical applications. Safety data should be consulted for handling and usage, as with any chemical substance.

Formula: C₁₅H₁₄O₄

InChI: InChI=1/C15H14O4/c1-18-15(17)13-8-7-12(9-14(13)16)19-10-11-5-3-2-4-6-11/h2-9,16H,10H2,1H3

SMILES: COC(=O)c1ccc(cc1O)OCc1ccccc1

2-Hydroxy-4-(phenylmethoxy)benzoic Acid Methyl Ester

CAS: 5427-29-2

2-Hydroxy-4-(phenylmethoxy)benzoic Acid Methyl Ester is a benzene derivative that inhibits the binding of xanthones to the benzene ring in a variety of ways. This compound is formed by reacting phenol with methyl benzoate in the presence of acid and heat. The low energy ligand inhibits the binding of xanthones to benzene by forming hydrogen bonds, covalent bonds, or van der Waals forces with the anion. 2-Hydroxy-4-(phenylmethoxy)benzoic acid methyl ester has shown anti-inflammatory properties, which may be due to its ability to inhibit leukocyte adhesion at inflammatory sites.

Formula: C₁₅H₁₄O₄

Purity: Min. 95%

Molecular weight: 258.27 g/mol

Ref: 3D-FAA42729