AB60736
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | in stock | $10.00 | $7.00 | - + | ||
1g | in stock | $16.00 | $12.00 | - + | ||
5g | in stock | $55.00 | $39.00 | - + | ||
10g | in stock | $100.00 | $70.00 | - + | ||
25g | 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.
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 |
Complexity: | 122 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 2 |
XLogP3: | 0.4 |
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.
Journal of the American Chemical Society 20120321
The Analyst 20111221
Acta crystallographica. Section E, Structure reports online 20111201
Acta crystallographica. Section E, Structure reports online 20110501
Acta crystallographica. Section E, Structure reports online 20110401
Acta crystallographica. Section E, Structure reports online 20110401
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110101
The journal of physical chemistry. A 20091224
International journal of biological macromolecules 20091101
Dalton transactions (Cambridge, England : 2003) 20090928
Inorganic chemistry 20081215
Inorganic chemistry 20080901
Inorganic chemistry 20080804
Dalton transactions (Cambridge, England : 2003) 20070928
The Journal of organic chemistry 20070831
Angewandte Chemie (International ed. in English) 20070101
The Journal of organic chemistry 20050930
Organic & biomolecular chemistry 20050907
Chemistry (Weinheim an der Bergstrasse, Germany) 20030905
The Journal of organic chemistry 20021004