4-Bromo-2-chloro-3-iodopyridine

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Reagent Code: #154944
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CAS Number 916203-52-6

science Other reagents with same CAS 916203-52-6

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scatter_plot Molecular Information
Weight 318.34 g/mol
Formula C₅H₂BrClIN
badge Registry Numbers
MDL Number MFCD08060939
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex pyridine-based structures. Commonly employed in medicinal chemistry for lead optimization due to the ease of functionalization. Also utilized in the preparation of ligands for catalysis and in materials science for designing organic semiconductors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,850.00
inventory 1g
10-20 days ฿15,280.00
inventory 5g
10-20 days ฿58,580.00

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4-Bromo-2-chloro-3-iodopyridine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex pyridine-based structures. Commonly employed in medicinal chemistry for lead optimization due to the ease of functionalization. Also utilized in the preparation of ligands for catalysis and i

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex pyridine-based structures. Commonly employed in medicinal chemistry for lead optimization due to the ease of functionalization. Also utilized in the preparation of ligands for catalysis and in materials science for designing organic semiconductors.

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