2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid

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Reagent Code: #91670
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CAS Number 2225177-12-6

science Other reagents with same CAS 2225177-12-6

blur_circular Chemical Specifications

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Weight 197.0144232 g/mol
Formula C₉H₁₃BFNO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound’s boronic acid group acts as a key functional group, enabling the formation of carbon-carbon bonds, which are essential for constructing active pharmaceutical ingredients (APIs). Its fluorine and tert-butyl substituents enhance its reactivity and selectivity, making it a valuable intermediate in the synthesis of biologically active compounds. Additionally, it is utilized in material science for the development of organic electronic materials and polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿135,200.00
inventory 5mg
10-20 days ฿10,520.00
inventory 25mg
10-20 days ฿45,060.00

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2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid
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2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound’s boronic acid group acts as a key functional group, enabling the formation of carbon-carbon bonds, which are essential for constructing active pharmaceutical ingredients (APIs). Its fluorine and tert-butyl substituents

2-Fluoro-6-(tert-butyl)pyridine-3-boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound’s boronic acid group acts as a key functional group, enabling the formation of carbon-carbon bonds, which are essential for constructing active pharmaceutical ingredients (APIs). Its fluorine and tert-butyl substituents enhance its reactivity and selectivity, making it a valuable intermediate in the synthesis of biologically active compounds. Additionally, it is utilized in material science for the development of organic electronic materials and polymers.

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