| Weight | 137.138 g/mol |
|---|---|
| Formula | C7H7NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Methyl isonicotinate (2459-09-8)
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- Synthesis, structural and spectroscopic study of polymeric copper(I) thiocyanato complexes [Cu(NCS)L]n (L=methyl nicotinate and ethyl nicotinate) and [HL][Cu(NCS)2] (HL=H-ethyl isonicotinate) (Polyhedron, 2000)
- The reduction mechanism of the >CO group: Part 1. The electrochemical reduction of methyl isonicotinate in an aqueous medium (Journal of Electroanalytical Chemistry, 1994)
- Arene-ruthenium(II) complexes containing 5-fluorouracil-1-methyl isonicotinate: Synthesis and characterization of their anticancer activity (Inorganica Chimica Acta, 2012)
- Basicity of the nitrogen atom and of the carbonyl function of methyl isonicotinate and 4-acetylpyridine. An infrared study of the interaction with proton donors (Journal of Heterocyclic Chemistry, 1985)
- Conformational studies by liquid crystal NMR and ab initio calculations: methyl nicotinate and methyl isonicotinate (Journal of Molecular Structure, 1992)
- Synthesis and Characterization of Cu(I) Complex Compounds With Methyl Isonicotinate (Canadian Journal of Chemistry, 1975)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)C1=CC=NC=C1
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InChIKeyOLXYLDUSSBULGU-UHFFFAOYSA-N
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Similar Compounds
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3-bromoisonicotinic acid
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4-(Methoxycarbonyl)nicotinic acid
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dimethyl pyridine-2,4-dicarboxylate
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2-ethylisonicotinic acid
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DIMETHYL TEREPHTHALATE
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ethyl quinoline-4-carboxylate
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ethyl 4-methyl-1h-pyrrole-3-carboxylate
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(71071-46-0)
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methyl 1h-indazole-6-carboxylate
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methyl isoquinoline-5-carboxylate
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2,6-Dimethoxyisonicotinic acid
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Methyl isonicotinate
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