5-Fluoro-2-(dimethylamino)pyridine-4-boronic acid

95%

Reagent Code: #58810
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CAS Number 2225174-59-2

science Other reagents with same CAS 2225174-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.9759032 g/mol
Formula C₇H₁₀BFN₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, the dimethylamino and fluorine substituents enhance its reactivity and selectivity, making it valuable for synthesizing biologically active compounds. It is also employed in the development of materials science applications, including the creation of advanced polymers and organic electronic materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿10,520.00
25mg
10-20 days ฿45,060.00
100mg
10-20 days ฿135,200.00
5-Fluoro-2-(dimethylamino)pyridine-4-boronic acid
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, the dimethylamino and fluorine substituents enhance its reactivity and selectivity, making it valuable for synthesizing

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, the dimethylamino and fluorine substituents enhance its reactivity and selectivity, making it valuable for synthesizing biologically active compounds. It is also employed in the development of materials science applications, including the creation of advanced polymers and organic electronic materials.

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