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

95%

Reagent Code: #92158
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CAS Number 2225180-41-4

science Other reagents with same CAS 2225180-41-4

blur_circular Chemical Specifications

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Weight 206.9694832 g/mol
Formula C₈H₇BFN₃O₂
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 building block for the introduction of fluorinated pyridine moieties into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The presence of both the imidazole and boronic acid groups enhances its reactivity and selectivity, making it a versatile intermediate in the synthesis of biologically active compounds. Additionally, its fluorinated structure can contribute to improved metabolic stability and bioavailability in drug design.

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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-(imidazol-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 building block for the introduction of fluorinated pyridine moieties into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The presence of both the imidazole and boronic acid groups enhances its reactivity and selectivity, making it a versatile intermediate in the synthesis of biologically active compou

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of fluorinated pyridine moieties into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The presence of both the imidazole and boronic acid groups enhances its reactivity and selectivity, making it a versatile intermediate in the synthesis of biologically active compounds. Additionally, its fluorinated structure can contribute to improved metabolic stability and bioavailability in drug design.

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