| Weight | 149.193 g/mol |
|---|---|
| Formula | C9H11NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
N-Ethylbenzamide (614-17-5)
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- Two Different Pathways of Stereoinformation Transfer: Asymmetric Substitutions in the ()-Sparteine Mediated Reactions of Laterally Lithiated N,N-Diisopropyl-o-ethylbenzamide and N-Pivaloyl-o-ethylaniline (Journal of the American Chemical Society, 1997)
- Regression of Dalton's lymphoma in vivo via decline in lactate dehydrogenase and induction of apoptosis by a ruthenium(II)-complex containing 4-carboxy N-ethylbenzamide as ligand (Investigational New Drugs, 2009)
- Ruthenium Complex as Enzyme Modulator: Modulation of Lactate Dehydrogenase by a Novel Ruthenium(II) Complex Containing 4-Carboxy N-Ethylbenzamide as a Ligand (Current Enzyme Inhibition, 2007)
- Activation of p53 mediated glycolytic inhibition-oxidative stress-apoptosis pathway in Dalton's lymphoma by a ruthenium (II)-complex containing 4-carboxy N-ethylbenzamide (Biochimie, 2015)
- Metabolites of N-ethylbenzamide, N,N-diethylbenzamide and related compounds detected in rat urine by NMR spectroscopy. (Drug Metabolism and Disposition, 1995)
- N-2-(2-pyridinyl) ethylbenzamide compounds and their use as fungicides (2004)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESCCNC(=O)C1=CC=CC=C1
-
InChIKeySDIDYFBTIZOPLA-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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N-Ethylbenzamide
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