| Weight | 102.089 g/mol |
|---|---|
| Formula | C4H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Ethyl glyoxalate (924-44-7)
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- Novel applications of ethyl glyoxalate with the Ugi MCR (Tetrahedron Letters, 1999)
- Nitroalkanes and Ethyl Glyoxalate as Common Precursors for the Preparation of Both -Keto Esters and ,-Unsaturated Esters. (Tetrahedron Letters, 2004)
- CopperCatalyzed Selective Oxidative Acylation of Secondary Anilines with Ethyl Glyoxalate: Domino Synthesis of Indoline2,3diones (Advanced Synthesis & Catalysis, 2013)
- A highly reactive carbonyl anion equivalent derived from ethyl glyoxalate and its conjugate addition to michael receptors (Tetrahedron Letters, 1973)
- Pd-catalyzed tandem cyclization of ethyl glyoxalate and amines: rapid assembly of highly substituted cyclic dehydro--amino acid derivatives. (Organic Letters, 2012)
- Polyfunctionalized pyrrolidinones via the coupling of N,N-disubstituted -amino esters with ethyl glyoxalate (Tetrahedron-asymmetry, 1998)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)C=O
-
InChIKeyDBPFRRFGLYGEJI-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Ethyl glyoxalate
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