5-Bromo-3-fluoro-2-methoxypyridine

98%

Reagent Code: #144990
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CAS Number 124432-70-8

science Other reagents with same CAS 124432-70-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.01 g/mol
Formula C₆H₅BrFNO
thermostat Physical Properties
Melting Point 40-43°C
Boiling Point 189.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory diseases and cancer. The presence of bromo and fluoro substituents enables sequential functionalization, offering flexibility in synthetic routes.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿6,850.00
inventory 100g
10-20 days ฿27,360.00
inventory 5g
10-20 days ฿1,800.00

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5-Bromo-3-fluoro-2-methoxypyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory diseases and cancer. The presence of bromo and fluoro substituents enables sequential functionaliz

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory diseases and cancer. The presence of bromo and fluoro substituents enables sequential functionalization, offering flexibility in synthetic routes.

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