| Weight | 107.112 g/mol |
|---|---|
| Formula | C6H5NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4-Pyridinecarboxaldehyde (872-85-5)
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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)
- Stereospecificity in the reductive coupling of 4-pyridinecarboxaldehyde (Journal of Organic Chemistry, 1981)
- Relationship between structure and antineoplastic activity of (arylsulfonyl)hydrazones of 4-pyridinecarboxaldehyde. (Journal of Medicinal Chemistry, 1985)
- A Study of the Structure: Mesogenic Behaviour Relationship in Three Types of Liquid Crystals (6-n-Alkoxy-3-Pyridinecarboxaldehyde Derivatives, 5-n-Alkoxy-2-Pyridinecarboxaldehyde Derivatives and 4-n-Alkoxybenzaldehyde Derivatives) Using Spectroscopic and Semi-Empirical Methods of Calculation (MNDO) (Molecular Crystals and Liquid Crystals, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=CC=C1C=O
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InChIKeyBGUWFUQJCDRPTL-UHFFFAOYSA-N
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