6-Bromo-4-fluoropyridin-3-ol

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Reagent Code: #130874
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CAS Number 1807007-85-7

science Other reagents with same CAS 1807007-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.99 g/mol
Formula C₅H₃BrFNO
badge Registry Numbers
MDL Number MFCD28739484
thermostat Physical Properties
Boiling Point 339.9±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.891±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

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 structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory and oncological diseases. The presence of both bromo and fluoro substituents enables sequential cross-coupling reactions, facilitating rapid diversification in compound libraries for drug discovery.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿41,400.00

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6-Bromo-4-fluoropyridin-3-ol
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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 structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory and oncological diseases. The presence of both bromo and fluoro substituents enables sequential cr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory and oncological diseases. The presence of both bromo and fluoro substituents enables sequential cross-coupling reactions, facilitating rapid diversification in compound libraries for drug discovery.

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