3-Bromo-2-iodo-5-methylpyridine

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Reagent Code: #154483
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CAS Number 1211542-16-3

science Other reagents with same CAS 1211542-16-3

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scatter_plot Molecular Information
Weight 297.92 g/mol
Formula C₆H₅BrIN
badge Registry Numbers
MDL Number MFCD16610048
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

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 molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance potency and selectivity. Also utilized in the preparation of functionalized heterocycles for use in crop protection agents and drug candidates targeting inflammatory and oncological diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,170.00
inventory 250mg
10-20 days ฿13,870.00
inventory 1g
10-20 days ฿45,950.00

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3-Bromo-2-iodo-5-methylpyridine
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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 molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance potency and selectivity. Also utilized in the preparation of functionalized heterocycles

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 molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance potency and selectivity. Also utilized in the preparation of functionalized heterocycles for use in crop protection agents and drug candidates targeting inflammatory and oncological diseases.

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