2-(3-Fluorophenyl)pyridine-4-boronic acid

95%

Reagent Code: #91481
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CAS Number 2225178-50-5

science Other reagents with same CAS 2225178-50-5

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Weight 217.0040632 g/mol
Formula C₁₁H₉BFNO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in pharmaceutical research. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for developing drug candidates and bioactive molecules. Additionally, it is utilized in material science for synthesizing advanced polymers and organic electronic materials. Its fluorophenyl group enhances its reactivity and stability, making it suitable for applications in medicinal chemistry and the development of fluorescent probes.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿29,700.00
inventory 100mg
10-20 days ฿82,800.00

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2-(3-Fluorophenyl)pyridine-4-boronic acid
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in pharmaceutical research. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for developing drug candidates and bioactive molecules. Additionally, it is utilized in material science for synthesizing advanced polymers and organic electronic materials. Its fluorophenyl group enh

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in pharmaceutical research. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for developing drug candidates and bioactive molecules. Additionally, it is utilized in material science for synthesizing advanced polymers and organic electronic materials. Its fluorophenyl group enhances its reactivity and stability, making it suitable for applications in medicinal chemistry and the development of fluorescent probes.

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