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

95%

Reagent Code: #92138
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CAS Number 2225176-35-0

science Other reagents with same CAS 2225176-35-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.9694832 g/mol
Formula C₈H₇BFN₃O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a versatile building block for creating complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in drug molecules. Additionally, the presence of the pyrazole and pyridine moieties enhances its potential in designing compounds with biological activity, such as kinase inhibitors or other therapeutic agents. Its application extends to materials science, where it can be utilized in the synthesis of organic electronic materials or ligands for catalysis.

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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-(1H-pyrazol-1-yl)pyridine-5-boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a versatile building block for creating complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in drug molecules. Additionally, the presence of the pyrazole and pyridine moieties enhances its potential in designing compounds

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a versatile building block for creating complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in drug molecules. Additionally, the presence of the pyrazole and pyridine moieties enhances its potential in designing compounds with biological activity, such as kinase inhibitors or other therapeutic agents. Its application extends to materials science, where it can be utilized in the synthesis of organic electronic materials or ligands for catalysis.

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