| Chemical Name: | 3-bromo-5-(2-chloropyridin-3-yl)pyridine |
| CAS Number: | 942206-00-0 |
| Product Number: | AG0065W8(AGN-PC-067UB2) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C10H6BrClN2 |
| Molecular Weight: | 269.5250 |
5′-Bromo-2-chloro-3,3′-bipyridine is a versatile compound commonly used in chemical synthesis for its unique reactivity and structural properties. It serves as a valuable building block in the preparation of complex organic molecules due to its functional groups and compatibility with various reactions. This compound is often employed in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its halogen substituents impart significant control over regioselectivity and allow for the introduction of further functional groups through cross-coupling reactions. Furthermore, 5′-Bromo-2-chloro-3,3′-bipyridine can participate in palladium-catalyzed coupling reactions, such as Suzuki-Miyaura and Heck reactions, to form biaryl compounds with high efficiency. Its presence in the molecule can also influence the electronic and steric properties of the final products, making it a valuable tool for fine-tuning the properties of target molecules.Overall, 5′-Bromo-2-chloro-3,3′-bipyridine plays a crucial role in modern organic synthesis by enabling the construction of complex molecular architectures with precise control over functionality and stereochemistry.
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(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
