4-Fluoro-2-(2-methylpiperidin-1-yl)pyridine-5-boronic acid

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Reagent Code: #92141
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CAS Number 2225152-70-3

science Other reagents with same CAS 2225152-70-3

blur_circular Chemical Specifications

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Weight 238.0663432 g/mol
Formula C₁₁H₁₆BFN₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized 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 research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures, which are common in drug molecules. Additionally, its fluorine substituent can enhance the metabolic stability and bioavailability of the resulting compounds, making it valuable in designing therapeutic agents.

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

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4-Fluoro-2-(2-methylpiperidin-1-yl)pyridine-5-boronic acid
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This compound is primarily utilized 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 research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures, which are common in drug molecules. Additionally, its fluorine substituent can enhance the metabolic stability and bioavailability of

This compound is primarily utilized 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 research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures, which are common in drug molecules. Additionally, its fluorine substituent can enhance the metabolic stability and bioavailability of the resulting compounds, making it valuable in designing therapeutic agents.

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