For research use only. Not for therapeutic Use.
Benzylmandelate(Cat No.:I014153) is a biochemical compound that belongs to the class of aromatic acids. It is derived from the combination of benzyl alcohol and mandelic acid. Benzylmandelate is commonly used in various biochemical and pharmaceutical applications. It serves as a precursor or intermediate in the synthesis of other organic compounds, including pharmaceutical drugs. Additionally, benzyl mandelate can be utilized as a chiral resolving agent, separating racemic mixtures into their enantiomers.
Catalog Number | I014153 |
CAS Number | 890-98-2 |
Synonyms | Benzylmandelate; NSC 9522; NSC-9522; NS 9522;Benzeneacetic acid, alpha-hydroxy-, phenylmethyl ester (9CI) |
Molecular Formula | C15H14O3 |
Purity | ≥95% |
Solubility | Soluble in DMSO |
IUPAC Name | benzyl 2-hydroxy-2-phenylacetate |
InChI | InChI=1S/C15H14O3/c16-14(13-9-5-2-6-10-13)15(17)18-11-12-7-3-1-4-8-12/h1-10,14,16H,11H2 |
InChIKey | JFKWZVQEMSKSBU-UHFFFAOYSA-N |
SMILES | C1=CC=C(C=C1)COC(=O)C(C2=CC=CC=C2)O |
Reference | </br> 1: Durand E, Lecomte J, Upasani R, Chabi B, Bayrasy C, Baréa B, Jublanc E, Clarke MJ, Moore DJ, Crowther J, Wrutniak-Cabello C, Villeneuve P. Evaluation of the ROS Inhibiting Activity and Mitochondrial Targeting of Phenolic Compounds in Fibroblast Cells Model System and Enhancement of Efficiency by Natural Deep Eutectic Solvent (NADES) Formulation. Pharm Res. 2017 May;34(5):1134-1146. doi: 10.1007/s11095-017-2124-4. Epub 2017 Feb 21. PubMed PMID: 28224387.</br>2: Friebolin V, Marten S, Albert K. Characterization of binding affinities in a chromatographic system by suspended state HR/MAS NMR spectroscopy. Magn Reson Chem. 2010 Feb;48(2):111-6. doi: 10.1002/mrc.2551. PubMed PMID: 19950216.</br></br> |