logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2,6-Pyridinedicarboxaldehyde

AB60736

5431-44-7 | 2,6-Pyridinedicarboxaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $10.00 $7.00 -   +
1g 98% in stock $16.00 $12.00 -   +
5g 98% in stock $55.00 $39.00 -   +
10g 98% in stock $100.00 $70.00 -   +
25g 98% in stock $244.00 $171.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB60736
Chemical Name: 2,6-Pyridinedicarboxaldehyde
CAS Number: 5431-44-7
Molecular Formula: C7H5NO2
Molecular Weight: 135.1201
MDL Number: MFCD00010103
SMILES: O=Cc1cccc(n1)C=O
NSC Number: 13393

 

Computed Properties
Complexity: 122  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 2  
XLogP3: 0.4  

 

 

Upstream Synthesis Route
  • 2,6-Pyridinedicarboxaldehyde, also known as 2,6-Pyridinedialdehyde, is a versatile chemical compound that finds wide applications in various chemical synthesis processes. This compound serves as a valuable building block in the synthesis of numerous organic compounds due to its unique structure and reactivity.One of the key applications of 2,6-Pyridinedicarboxaldehyde is its role as a precursor in the synthesis of heterocyclic compounds. Its aldehyde functional groups can undergo various chemical transformations, such as condensation reactions, to form complex heterocycles with nitrogen-containing rings. These heterocyclic compounds are widely used in pharmaceuticals, agrochemicals, and materials science.Additionally, 2,6-Pyridinedicarboxaldehyde is utilized in the preparation of fluorescent dyes and sensors. Its aromatic structure and aldehyde groups make it a suitable candidate for derivatization to design fluorescent molecules for bioimaging, sensing, and analytical applications. By modifying its structure, researchers can tailor its properties for specific sensing or imaging purposes.Moreover, 2,6-Pyridinedicarboxaldehyde is employed in the synthesis of coordination compounds and metal-organic frameworks (MOFs). Its ability to chelate metal ions allows for the formation of stable coordination complexes with a variety of metals. These complexes have various applications in catalysis, material science, and molecular recognition due to their unique structures and properties.Overall, 2,6-Pyridinedicarboxaldehyde plays a crucial role in advancing chemical synthesis by serving as a versatile building block for the construction of diverse organic compounds with applications ranging from drug discovery to materials science and beyond.
Literature
FEATURED PRODUCTS