(6-Cyano-5-fluoropyridin-3-yl)boronic acid

95%

Reagent Code: #131660
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CAS Number 2407353-18-6

science Other reagents with same CAS 2407353-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.92 g/mol
Formula C₆H₄BFN₂O₂
badge Registry Numbers
MDL Number MFCD18260336
thermostat Physical Properties
Boiling Point 386.8±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.44±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient formation of carbon-carbon bonds in heterocyclic systems. The presence of fluorine and cyano groups enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of compounds targeting cancer, inflammation, and central nervous system disorders. Its structural features make it valuable in medicinal chemistry for optimizing potency and pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,900.00
inventory 250mg
10-20 days ฿4,990.00
inventory 1g
10-20 days ฿13,300.00

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(6-Cyano-5-fluoropyridin-3-yl)boronic acid
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Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient formation of carbon-carbon bonds in heterocyclic systems. The presence of fluorine and cyano groups enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of compounds targeting cancer, inflammation, and central nervous sys

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient formation of carbon-carbon bonds in heterocyclic systems. The presence of fluorine and cyano groups enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of compounds targeting cancer, inflammation, and central nervous system disorders. Its structural features make it valuable in medicinal chemistry for optimizing potency and pharmacokinetic properties.

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