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

95%

Reagent Code: #187639
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CAS Number 452972-14-4

science Other reagents with same CAS 452972-14-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.05 g/mol
Formula C₁₁H₁₅BFNO₂
badge Registry Numbers
MDL Number MFCD06798245
thermostat Physical Properties
Melting Point 42-45°C
Boiling Point 309.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in medicinal chemistry for constructing complex pyridine-based structures found in bioactive molecules. It is also employed in materials science for developing organic semiconductors and functional molecules requiring tailored electronic properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,030.00
inventory 25g
10-20 days ฿5,010.00
inventory 100g
10-20 days ฿19,510.00

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2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in medicinal chemistry for constructing complex pyridine-based structures found in bioactive molecules. It is also employed in materials science for developing organic semiconductors and functional molecules requiring tailored electronic properties.
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