AA14544
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 96% | in stock | $63.00 | $44.00 | - + | |
250mg | 96% | in stock | $76.00 | $53.00 | - + | |
1g | 96% | in stock | $89.00 | $62.00 | - + | |
5g | 96% | in stock | $233.00 | $163.00 | - + | |
10g | 96% | in stock | $386.00 | $270.00 | - + | |
25g | 96% | in stock | $743.00 | $520.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA14544 |
Chemical Name: | 2,6-Dibromo-4-iodopyridine |
CAS Number: | 1160184-14-4 |
Molecular Formula: | C5H2Br2IN |
Molecular Weight: | 362.7885 |
MDL Number: | MFCD13185521 |
SMILES: | Ic1cc(Br)nc(c1)Br |
Complexity: | 91 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 1 |
XLogP3: | 3.6 |
2,6-Dibromo-4-iodopyridine is a versatile compound used in various chemical synthesis processes. It serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and materials. This compound specifically plays a crucial role in the synthesis of complex organic molecules due to its unique reactivity pattern and structural features.In organic chemistry, 2,6-Dibromo-4-iodopyridine is frequently employed as a key intermediate for constructing heterocyclic frameworks in drug discovery and development. Its ability to undergo selective functionalization reactions makes it a valuable tool for creating diverse molecular structures with specific biological activities.Furthermore, 2,6-Dibromo-4-iodopyridine is utilized in the preparation of ligands for metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Heck couplings. These reactions are essential in the formation of carbon-carbon and carbon-heteroatom bonds, enabling the synthesis of complex organic molecules with high efficiency and selectivity.Overall, the unique properties of 2,6-Dibromo-4-iodopyridine make it an indispensable component in the toolkit of synthetic chemists, driving innovation and advancements in the field of chemical synthesis.