Ethyl Mandelate

CAS : 774-40-3

Ref. TR-E922055

Informations sur le produit

• Nom: Ethyl Mandelate
• Synonymes: alpha-Hydroxybenzeneacetic acid ethyl ester, Mandelic acid, ethyl ester (6CI,7CI,8CI), (+/-)-Mandelic acid ethyl ester, (+/-)-alpha-Hydroxybenzeneacetic acid ethyl ester, DL-Ethyl mandelate, DL-Mandelic acid ethyl ester, Ethyl 2-hydroxy-2-phenylacetate, Ethyl amygdalate, Ethyl hydroxy(phenyl)acetate, Ethyl phenylglycolate, Ethyl alpha-hydroxybenzeneacetate, Ethyl alpha-hydroxyphenylacetate, NSC 5307, dl-Mandelic acid ethyl ester, (±)-α-Hydroxybenzeneacetic acid ethyl ester, <span class="text-smallcaps">D</smallcap><smallcap>L</span>-Ethyl mandelate, <span class="text-smallcaps">D</smallcap><smallcap>L</span>-Mandelic acid ethyl ester, Benzeneacetic acid, alpha-hydroxy-, ethyl ester, Benzeneacetic acid, α-hydroxy-, ethyl ester, Ethyl 2-phenyl-2-hydroxyacetate, Ethyl Hydroxy(Phenyl)Acetate, Ethyl α-hydroxybenzeneacetate, Ethyl α-hydroxyphenylacetate, Ethylphenylglycolate, Mandelic Acid Ethyl Ester

Description

Applications Ethyl Mandelate is used as a reagent in the synthesis of several organic compounds including that of volatile methylsiloxanes which have the potential to be a more environmentally sustainable alternative as solvents in chemical synthesis to non-polar organic solvents. It was found to act as a substrate for (S)-mandelate dehydrogenase which is a flavin mononucleotide dependent enzyme that oxidises (S)-mandelate to benzoylformate.
References Ab Rani, M., et al.: Green Chem., 16, 282 (2014); Dewanti, A., et al.: Biochemistry-US, 43, 1883 (2004);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 180.20
• Formule: C₁₀H₁₂O₃
• Couleur/Forme: Colourless Oil
• InChI: InChI=1S/C10H12O3/c1-2-13-10(12)9(11)8-6-4-3-5-7-8/h3-7,9,11H,2H2,1H3
• Code InChI: InChIKey=SAXHIDRUJXPDOD-UHFFFAOYSA-N
• SMILES: CCOC(=O)C(O)c1ccccc1