| Weight | 165.192 g/mol |
|---|---|
| Formula | C9H11NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Ethyl 2-pyridylacetate (2739-98-2)
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- Synthesis of a Series of Derivatives of Ethyl 2-Pyridylacetate (Journal of Organic Chemistry, 1961)
- A Convenient Preparation of Ethyl 2-Pyridylacetate (Journal of the American Chemical Society, 1953)
- 507. Preparation of indolizines from ethyl 2-pyridylacetate (Journal of The Chemical Society (resumed), 1962)
- 1004. Condensation of ethyl 2- and 4-pyridylacetate with aromatic carbonyl compounds (Journal of The Chemical Society (resumed), 1961)
- Instances of non-electrolyte solvation leading to less pronounced rate enhancements of ester hydrolyses in dipolar aprotic solvents: the possibility of hydrolysis via conjugate base formation in the case of ethyl indole-2-carboxylate and methyl 4-pyridylacetate (Journal of The Chemical Society-perkin Transactions 1, 1978)
- Preparation of indolizines from ethyl bromopyruvate and ethyl 2-pyridylacetate (Journal of The Chemical Society C: Organic, 1966)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)CC1=CC=CC=N1
-
InChIKeyIUDKTVXSXWAKJO-UHFFFAOYSA-N
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Synthesis
Reactant
+
Ethanol
(O-acylation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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29800-89-3
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(1-Methyl-1H-pyrrol-2-yl)(oxo)acetic acid
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2-BROMO-6-ISOPROPYLPYRIDINE
(1037223-35-0)
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Ethyl 2-pyridylacetate
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