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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2,6-Dibromo-4-iodopyridine

AA14544

1160184-14-4 | 2,6-Dibromo-4-iodopyridine

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 -   +

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*All prices are in USD.

Description
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

 

Computed Properties
Complexity: 91  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 1  
XLogP3: 3.6  

 

 

Upstream Synthesis Route
  • 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.
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