4-Fluoro-2-(4-methyl-1H-pyrazol-1-yl)pyridine-5-boronic acid

95%

Reagent Code: #92145
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CAS Number 2225169-40-2

science Other reagents with same CAS 2225169-40-2

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Weight 220.9960632 g/mol
Formula C₉H₉BFN₃O₂
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 Suzuki-Miyaura coupling. Its boronic acid group enables it to act as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. The presence of the pyrazole and pyridine rings enhances its ability to interact with biological targets, making it valuable in drug discovery for designing compounds with potential therapeutic effects. Additionally, its fluorine substituent can influence the metabolic stability and binding affinity of the resulting molecules, further expanding its applications in medicinal chemistry.

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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-(4-methyl-1H-pyrazol-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 Suzuki-Miyaura coupling. Its boronic acid group enables it to act as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. The presence of the pyrazole and pyridine rings enhances its ability to interact with biological targets, making it valuable in drug discovery for designing compounds with potential therapeutic effects. A

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid group enables it to act as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. The presence of the pyrazole and pyridine rings enhances its ability to interact with biological targets, making it valuable in drug discovery for designing compounds with potential therapeutic effects. Additionally, its fluorine substituent can influence the metabolic stability and binding affinity of the resulting molecules, further expanding its applications in medicinal chemistry.

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