4-Bromo-6-chloro-3-iodo-2-methylpyridine

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Reagent Code: #150754
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CAS Number 1809161-45-2

science Other reagents with same CAS 1809161-45-2

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scatter_plot Molecular Information
Weight 332.36 g/mol
Formula C₆H₄BrClIN
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MDL Number MFCD28154571
inventory_2 Storage & Handling
Storage Store at room temperature away from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic structures. Commonly employed in medicinal chemistry for lead optimization due to the ease of functionalization at multiple halogen sites. 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 100mg
10-20 days ฿13,250.00
inventory 250mg
10-20 days ฿21,800.00
inventory 1g
10-20 days ฿43,610.00

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4-Bromo-6-chloro-3-iodo-2-methylpyridine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic structures. Commonly employed in medicinal chemistry for lead optimization due to the ease of functionalization at multiple halogen sites. Also utilized in the preparation of ligands for catalysis

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

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