| Names | |
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Preferred IUPAC name
Pyridine-2-carbaldehyde
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| Other names
Picolinaldehyde
2-Pyridine carboxaldehyde 2-Pyridyl aldehyde Picolinal |
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| Identifiers | |
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3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.013.031 |
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PubChem CID
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| Properties | |
| C6H5NO | |
| Molar mass | 107.11 g·mol−1 |
| Density | 1.126 g/mL |
| Boiling point | 181 °C (358 °F; 454 K) |
| Related compounds | |
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Related Aldehydes
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Salicylaldehyde Quinoline Carboxaldehyde |
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Related compounds
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Picolinic acid |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
2-Formylpyridine, also commonly called pyridine-2-carboxaldehyde, is an organic compound with the formula NC5H4CHO. It is a colorless oily liquid with a distinctive odor. Older samples are often brown-colored owing to impurities. It serves as a precursor to other compounds of interest in coordination chemistry and pharmaceuticals. Pyridine aldehydes are typically prepared by oxidation of the hydroxymethyl- or methylpyridines.
The drug pralidoxime can be produced from 2-formylpyridine.
The aldehyde functional group is subject to nucleophilic attack, specifically by amines to form Schiff bases, which serve as bidentate ligands. Iminopyridine complexes can be remarkably robust.