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234111-08-1

Pyridine, 2-bromo-6-iodo-

Catalog#: AR002NUM  |   CAS#: 234111-08-1  |   MDL#: MFCD08059557  |   MF: C5H3BrIN  |   MW: 283.8925

Packsize Purity Price Availability Quantity
100mg 98% $3.00 Global Stock Buy Now Add To Cart
250mg 98% $5.00 Global Stock Buy Now Add To Cart
1g 98% $11.00 Global Stock Buy Now Add To Cart
5g 98% $42.00 Global Stock Buy Now Add To Cart
10g 98% $74.00 Global Stock Buy Now Add To Cart
25g 98% $169.00 Global Stock Buy Now Add To Cart
100g 98% $674.00 Global Stock Buy Now Add To Cart
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Catalog Number AR002NUM
Chemical Name Pyridine, 2-bromo-6-iodo-
CAS Number 234111-08-1
Molecular Formula C5H3BrIN
Molecular Weight 283.8925
MDL Number MFCD08059557
SMILES Brc1cccc(n1)I

2-Bromo-6-iodopyridine is a versatile chemical compound that finds widespread application in chemical synthesis. This compound serves as a valuable building block in organic chemistry due to its unique reactivity and functional group compatibility. In particular, 2-Bromo-6-iodopyridine is commonly used in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.One prominent application of 2-Bromo-6-iodopyridine is in the preparation of heterocyclic compounds. By utilizing its halogen substituents, chemists can efficiently introduce structural complexity and diversity into target molecules. Additionally, the presence of both bromine and iodine atoms enables selective functionalization at specific positions within the pyridine ring, allowing for precise manipulation of chemical structures.Furthermore, 2-Bromo-6-iodopyridine serves as a convenient source of cross-coupling reactions in transition-metal catalyzed processes. Its halogen substituents facilitate palladium-catalyzed coupling reactions with a variety of organometallic reagents, enabling the synthesis of complex molecules with high efficiency and selectivity. This compound is particularly valuable in the construction of carbon-carbon and carbon-heteroatom bonds, which are essential in the preparation of bioactive compounds and synthetic intermediates.Overall, the versatility and reactivity of 2-Bromo-6-iodopyridine make it an indispensable tool for chemists engaged in organic synthesis. Its strategic use in chemical transformations allows for the rapid and efficient construction of molecular scaffolds with diverse applications in the fields of medicine, agriculture, and materials science.
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