2-Bromo-3-iodo-6-methylpyridine

96%

Reagent Code: #151405
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CAS Number 1227579-03-4

science Other reagents with same CAS 1227579-03-4

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scatter_plot Molecular Information
Weight 297.92 g/mol
Formula C₆H₅BrIN
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MDL Number MFCD16610044
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

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, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in Suzuki, Stille, and Negishi couplings to introduce aryl or alkyl groups during drug discovery processes. Also utilized in the preparation of functionalized pyridine derivatives that serve as key scaffolds in advanced organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,270.00
inventory 250mg
10-20 days ฿7,900.00
inventory 1g
10-20 days ฿19,730.00

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2-Bromo-3-iodo-6-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, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in Suzuki, Stille, and Negishi couplings to introduce aryl or alkyl groups during drug discovery processes. Also utilized in the preparation of functionalized pyridine deriv

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, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in Suzuki, Stille, and Negishi couplings to introduce aryl or alkyl groups during drug discovery processes. Also utilized in the preparation of functionalized pyridine derivatives that serve as key scaffolds in advanced organic synthesis.

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