| Weight | 180.203 g/mol |
|---|---|
| Formula | C10H12O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
ETHYL MANDELATE (4358-88-7, 774-40-3)
ethyl mandelate, (R)-isomer · ethyl mandelate, (+-)-isomer · ethyl mandelate, (S)-isomer
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- Polymer and Silica Supported Tridentate Schiff Base Vanadium Catalysts for the Asymmetric Oxidation of Ethyl Mandelate Activity, Stability and Recyclability (Advanced Synthesis & Catalysis, 2008)
- SuzukiMiyaura Coupling Reaction of Boronic Acids and Ethyl Glyoxylate: Synthetic Access to Mandelate Derivatives (European Journal of Organic Chemistry, 2008)
- Hydrolytic resolution of (R,S)-ethyl mandelate in biphasic media via Klebsiella oxytoca hydrolase (Enzyme and Microbial Technology, 2005)
- Enantioselective catalytic synthesis of ethyl mandelate derivatives using Rh(I)NHC catalysts and organoboron reagents (Tetrahedron-asymmetry, 2013)
- L.Catalytic racemisation of ethyl l-mandelate (Journal of The Chemical Society, Transactions, 1919)
- 33. Experiments on the interaction of hydroxy-compounds and phosphorus and thionyl halides in the absence and in the presence of tertiary bases. Part I. Optically active -octanol, ethyl mandelate, and phenylmethylcarbinol (Journal of The Chemical Society (resumed), 1944)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ethyl mandelate, (R)-isomer
- ethyl mandelate, (+-)-isomer
- ethyl mandelate, (S)-isomer
-
SMILESCCOC(=O)C(C1=CC=CC=C1)O
-
InChIKeySAXHIDRUJXPDOD-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
benzene
+
Reactant
(Friedel-Crafts alkylation)
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ETHYL MANDELATE
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