Pyridine-2,3-dicarbaldehyde
Names and Identifiers of Pyridine-2,3-dicarbaldehyde
CAS Number |
4663-93-8 |
|---|---|
IUPAC Name |
pyridine-2,3-dicarbaldehyde |
InChI |
InChI=1S/C7H5NO2/c9-4-6-2-1-3-8-7(6)5-10/h1-5H |
InChIKey |
OYBLXLFKRJWZJG-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC(=C(N=C1)C=O)C=O |
Physical and chemical properties of Pyridine-2,3-dicarbaldehyde
Boiling Point |
277.435ºC at 760 mmHg |
|---|---|
Density |
1.275 g/cm3 |
Exact Mass |
135.03200 |
Flash Point |
125.795ºC |
LogP |
0.70660 |
Molecular Formula |
C7H5NO2 |
Molecular Weight |
135.12000 |
PSA |
47.03000 |
Applications of Pyridine-2,3-dicarbaldehyde
Pyridine-2,3-dicarbaldehyde has diverse applications across various fields:
- Chemical Industry: It serves as a building block for synthesizing complex organic molecules and heterocyclic compounds.
- Pharmaceuticals: It is used as a precursor for biologically active molecules and potential drug candidates.
- Dyes and Pigments: The compound is also utilized in the production of functionalized resins and intermediates for dyes.
Interaction Studies of Pyridine-2,3-dicarbaldehyde
Studies focusing on the interactions of pyridine-2,3-dicarbaldehyde with other compounds have revealed its ability to react with nitrogen nucleophiles. These interactions can lead to the formation of various derivatives that may exhibit enhanced biological activity or novel properties. Research continues to explore these interactions to develop new applications in medicinal chemistry and materials science.
Biological Activity of Pyridine-2,3-dicarbaldehyde
Research indicates that pyridine-2,3-dicarbaldehyde and its derivatives exhibit significant biological activity. They have been investigated for their potential as pharmaceuticals, particularly due to their ability to form Schiff bases with bioactive amines. This property suggests potential applications in drug development targeting various biological pathways. Studies have also explored their antimicrobial properties and interactions with biological macromolecules.