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Structure of 502509-20-8
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4-Bromo-2-vinylpyridine features a vinyl group conjugated to a pyridine ring, enabling efficient copolymerization and cross-coupling reactions. The bromine substituent provides a reactive handle for palladium-catalyzed transformations, while the nitrogen atom enhances solubility and facilitates coordination in catalytic systems. This compound serves as a key building block in functional materials and pharmaceutical intermediates.
4-Bromo-2-vinylpyridine serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling the construction of conjugated biaryl and styryl architectures. The vinyl group facilitates efficient Heck, Suzuki-Miyaura, and Sonogashira couplings, while the bromide supports palladium-catalyzed transformations. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical choice for synthesizing complex heterocyclic scaffolds and advanced intermediates in medicinal chemistry and materials science.
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Lot numbers can be found on the outside label of a product: