2-Fluoro-6-(cyclobutyl)pyridine-3-boronic acid

95%

Reagent Code: #91645
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CAS Number 2225178-14-1

science Other reagents with same CAS 2225178-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.9985432 g/mol
Formula C₉H₁₁BFNO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This property is particularly valuable in constructing complex molecules, such as active pharmaceutical ingredients (APIs) or biologically active compounds. Additionally, the fluorine atom in its structure can enhance the metabolic stability and binding affinity of the resulting molecules, making it useful in drug discovery and development processes. Its cyclobutyl group may also contribute to the steric and electronic properties of the final product, influencing its biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿135,200.00
inventory 5mg
10-20 days ฿10,520.00
inventory 25mg
10-20 days ฿45,060.00

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2-Fluoro-6-(cyclobutyl)pyridine-3-boronic acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This property is particularly valuable in constructing complex molecules, such as active pharmaceutical ingredients (APIs) or biologically active compounds. Additionally, the fluorine atom in its structure can enhance the metabo

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This property is particularly valuable in constructing complex molecules, such as active pharmaceutical ingredients (APIs) or biologically active compounds. Additionally, the fluorine atom in its structure can enhance the metabolic stability and binding affinity of the resulting molecules, making it useful in drug discovery and development processes. Its cyclobutyl group may also contribute to the steric and electronic properties of the final product, influencing its biological activity.

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