3-Fluoro-2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

≥95%

Reagent Code: #130431
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CAS Number 1220696-64-9

science Other reagents with same CAS 1220696-64-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.08 g/mol
Formula C₁₂H₁₇BFNO₂
badge Registry Numbers
MDL Number MFCD18382856
thermostat Physical Properties
Boiling Point 300.1±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.08±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active pyridine derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. Commonly employed in the development of kinase inhibitors and other drug candidates where fluorinated and methylated pyridine scaffolds enhance metabolic stability and binding affinity. Also applied in materials science for constructing conjugated systems in organic electronics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,250.00
inventory 1g
10-20 days ฿16,500.00

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3-Fluoro-2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active pyridine derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. Commonly employed in the development of kinase inhibitors and other drug candidates where fluorinated and methylated pyridine scaffolds enhance metabolic stability and binding affinity. Also applied in materials science for constructing co

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active pyridine derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. Commonly employed in the development of kinase inhibitors and other drug candidates where fluorinated and methylated pyridine scaffolds enhance metabolic stability and binding affinity. Also applied in materials science for constructing conjugated systems in organic electronics.

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