| Weight | 206.194 g/mol |
|---|---|
| Formula | C8H14O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Diethyl tartrate (87-91-2, 57968-71-5)
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- Asymmetric conjugate addition of diethyl zinc to enones with tartrate chiral phosphite ligands (Tetrahedron-asymmetry, 1997)
- Synthesis of enantiomerically enriched homoallylic alcohols and of 1,2-dien-1-ols using chiral tin(IV) complexes containing diethyl tartrate as an auxiliary ligand (Journal of Organic Chemistry, 1987)
- A Practical and Azide-Free Synthetic Approach to Oseltamivir from Diethyl d-Tartrate (Journal of Organic Chemistry, 2010)
- Transacetalization of Diethyl Tartrate with Acetals of .alpha.-Dicarbonyl Compounds: A Simple Access to a New Class of C2-Symmetric Auxiliaries and Ligands (Journal of Organic Chemistry, 1995)
- An enantioselective total synthesis of (+)-altholactone from diethyl L-tartrate (Tetrahedron, 1994)
- A new and concise synthetic route to an enantiopure (+)-conduritol-E derivative from diethyl l-tartrate (Tetrahedron-asymmetry, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)C(C(C(=O)OCC)O)O
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InChIKeyYSAVZVORKRDODB-UHFFFAOYSA-N
- Pubchem - Diethyl tartrate
- Wikipedia - Diethyl tartrate
Diethyl tartrate is an organic compound, the ethyl ester of tartaric acid. It exists in both as a chiral isomer, showing both left- and right-handed forms, as well as a meso stereoisomer, which is not chiral. The chiral isomer is far more common.
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Synthesis
Ethyl glyoxalate
+
Reactant
(Grignard alcohol)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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