CAS 295320-25-1
:Benzyl 3-hydroxyphenylacetate
Description:
Benzyl 3-hydroxyphenylacetate, identified by its CAS number 295320-25-1, is an organic compound characterized by its ester functional group. It is derived from the reaction of benzyl alcohol and 3-hydroxyphenylacetic acid. This compound typically appears as a colorless to pale yellow liquid with a pleasant aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the hydroxyl group contributes to its potential for hydrogen bonding, influencing its reactivity and interactions with other substances. Benzyl 3-hydroxyphenylacetate may exhibit biological activity, making it of interest in various fields, including pharmaceuticals and fragrance formulations. Its stability and reactivity can be affected by factors such as temperature and pH, which are important considerations in its handling and application. Overall, this compound is notable for its aromatic properties and potential utility in diverse chemical applications.
Formula:C15H14O3
InChI:InChI=1/C15H14O3/c16-14-8-4-7-13(9-14)10-15(17)18-11-12-5-2-1-3-6-12/h1-9,16H,10-11H2
SMILES:c1ccc(cc1)COC(=O)Cc1cccc(c1)O
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Found 5 products.
Benzyl 3-hydroxyphenylacetate, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C15H14O3Purity:98%Color and Shape:Powder, Cream to pale brownMolecular weight:242.27Benzeneacetic acid, 3-hydroxy-, phenylmethyl ester
CAS:Formula:C15H14O3Purity:95%Color and Shape:SolidMolecular weight:242.2699Benzyl 2-(3-Hydroxyphenyl)Acetate
CAS:Benzyl 2-(3-Hydroxyphenyl)AcetatePurity:98%Molecular weight:242.27g/molBenzyl 2-(3-Hydroxyphenyl)acetate
CAS:Controlled Product<p>Applications Benzyl 2-(3-Hydroxyphenyl)acetate is a regent in the synthesis of Nahlsgen (N497063) which is a highly selective, and irreversible γ-glutamyl transpeptidase (GGT) inhibitor with no inhibitory activity on glutamine amidotransferases.<br>References Yamamoto, S., et al.: J. Pharmacol. Exp. Ther., 339, 945 (2011); Tuzova, M., et al.: Front Pharmacol., 5, 1, 2014<br></p>Formula:C15H14O3Color and Shape:NeatMolecular weight:242.27




