| Weight | 164.16 g/mol |
|---|---|
| Formula | C9H8O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Methyl benzoylformate (81065-82-9, 15206-55-0)
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- Asymmetric Hydrogenation of Methyl Benzoylformate Using Platinum-Carbon Catalysts Modified with Cinchonidine (Journal of Synthetic Organic Chemistry Japan, 1979)
- Reduction by a Model of NAD(P)H. XV. Kinetics for the Reduction of Methyl Benzoylformate (Bulletin of the Chemical Society of Japan, 1977)
- Model complexes for .alpha.-keto acid-dependent enzymes. Structure and reactivity of {FeII[tris[(6-methyl-2-pyridyl)methyl]amine](benzoylformate)}(ClO4) (Journal of the American Chemical Society, 1992)
- Highly reactive and stereospecific reaction of quinoline-type NADH model compounds with methyl benzoylformate (Tetrahedron Letters, 2000)
- Chiral organometallic NADH mimics: Preparation of homochiral (R)-()[(5-c5h5)fe(co)(pph2(o-(l)-menthyl1))]-1-methyl-1,4-dihydronicotinand asymmetric reduction of ethyl benzoylformate. (Tetrahedron Letters, 1990)
- Pyrolysis of hydroxyketones and ketoesters: Gasphase elimination kinetics of 3hydroxy3methyl2butanone and methyl benzoylformate (International Journal of Chemical Kinetics, 1997)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)C(=O)C1=CC=CC=C1
-
InChIKeyYLHXLHGIAMFFBU-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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Methyl benzoylformate
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