2-Bromo-5-iodo-4-methylpyridine

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Reagent Code: #146460
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CAS Number 942206-07-7

science Other reagents with same CAS 942206-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.92 g/mol
Formula C₆H₅BrIN
thermostat Physical Properties
Melting Point 50-52°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an 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 aromatic systems. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the ease of functionalization at the bromo and iodo 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 5g
10-20 days ฿3,430.00
inventory 25g
10-20 days ฿16,710.00
inventory 100g
10-20 days ฿64,000.00

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2-Bromo-5-iodo-4-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 biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the ease of functionalization at the bromo and iodo sites. Also utilized in the prep

Used as an 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 aromatic systems. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the ease of functionalization at the bromo and iodo sites. Also utilized in the preparation of ligands for catalysis and in materials science for designing organic semiconductors.

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