3-Methyl-1-(pyridin-3-yl)pyrazole-4-boronic acid

95%

Reagent Code: #90091
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CAS Number 1394837-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.0056 g/mol
Formula C₉H₁₀BN₃O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

3-Methyl-1-(pyridin-3-yl)pyrazole-4-boronic acid is primarily used in organic synthesis as a key building block for the preparation of more complex molecules. Its boronic acid functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create carbon-carbon bonds. This compound is particularly useful in the development of drug candidates, as it allows for the efficient construction of biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it finds applications in material science, where it is used to synthesize organic electronic materials and polymers with specific properties. Its pyrazole and pyridine moieties also contribute to its utility in designing ligands for catalysis and coordination chemistry.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days $358.18
inventory 25mg
10-20 days $789.58
3-Methyl-1-(pyridin-3-yl)pyrazole-4-boronic acid
3-Methyl-1-(pyridin-3-yl)pyrazole-4-boronic acid is primarily used in organic synthesis as a key building block for the preparation of more complex molecules. Its boronic acid functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create carbon-carbon bonds. This compound is particularly useful in the development of drug candidates, as it allows for the efficient construction of biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it finds applications in material science, where it is used to synthesize organic electronic materials and polymers with specific properties. Its pyrazole and pyridine moieties also contribute to its utility in designing ligands for catalysis and coordination chemistry.
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