| Weight | 107.112 g/mol |
|---|---|
| Formula | C6H5NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-Pyridinecarboxaldehyde (500-22-1)
3-pyridinaldehyde · nicotinaldehyde
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- Synthesis of Isoquinoline Alkaloids. II. The Synthesis and Reactions of 4-Methyl-3-pyridinecarboxaldehyde and Other 4-Methyl-3-substituted Pyridines1,2 (Journal of Organic Chemistry, 1960)
- Synthesis and spectroscopic properties of Schiff bases derived from 3-hydroxy-4-pyridinecarboxaldehyde (Tetrahedron, 2005)
- Kinetic study of the hydration reaction of 2-, 3-, and 4-pyridinecarboxaldehyde (The Journal of Physical Chemistry, 1972)
- 3-Pyridinecarboxaldehyde: A Model System for Superelectrophilic Activation and the Observation of a Diprotonated Electrophile (Journal of Organic Chemistry, 1999)
- Anti-Tubercular Activity in vivo of Nicotinaldehyde Thiosemicarbazone and its Isomers. (Experimental Biology and Medicine, 1951)
- Pentadentate ligands. II. Nickel(II) complexes of the linear Schiff base ligand derived from 2-pyridinecarboxaldehyde and bis(3,3'-aminopropyl)amine (Inorganic Chemistry, 1971)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-pyridinaldehyde
- nicotinaldehyde
-
SMILESC1=CC(=CN=C1)C=O
-
InChIKeyQJZUKDFHGGYHMC-UHFFFAOYSA-N
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