(2-Fluoro-3-methoxypyridin-4-yl)boronic acid

97%

Reagent Code: #131107
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CAS Number 1451392-01-0

science Other reagents with same CAS 1451392-01-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.93 g/mol
Formula C₆H₇BFNO₃
badge Registry Numbers
MDL Number MFCD16611242
thermostat Physical Properties
Boiling Point 381.5±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.34±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecules. Commonly employed in the preparation of drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. The presence of fluorine and methoxy groups enhances binding selectivity and metabolic stability in final active ingredients. Widely utilized in medicinal chemistry for lead optimization due to its favorable reactivity and structural features.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,400.00
inventory 1g
10-20 days ฿35,000.00

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(2-Fluoro-3-methoxypyridin-4-yl)boronic acid
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Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecules. Commonly employed in the preparation of drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. The presence of fluorine and methoxy groups enhan

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecules. Commonly employed in the preparation of drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. The presence of fluorine and methoxy groups enhances binding selectivity and metabolic stability in final active ingredients. Widely utilized in medicinal chemistry for lead optimization due to its favorable reactivity and structural features.

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