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

≥95%

Reagent Code: #130491
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CAS Number 1351997-55-1

science Other reagents with same CAS 1351997-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.14 g/mol
Formula C₁₂H₁₇BFNO₄S
badge Registry Numbers
MDL Number MFCD18753415
thermostat Physical Properties
Boiling Point 432.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.26±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

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. The fluorine and methylsulfonyl substituents enhance reactivity and direct regioselectivity in coupling processes, allowing precise construction of complex molecules. Commonly employed in the development of kinase inhibitors and other therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,920.00
inventory 250mg
10-20 days ฿13,470.00

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3-Fluoro-2-(methylsulfonyl)-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. The fluorine and methylsulfonyl substituents enhance reactivity and direct regioselectivity in coupling processes, allowing precise construction of complex molecules. Commonly employed in the development of kinase inhibitors and other ther

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. The fluorine and methylsulfonyl substituents enhance reactivity and direct regioselectivity in coupling processes, allowing precise construction of complex molecules. Commonly employed in the development of kinase inhibitors and other therapeutic agents.

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