(5-(1-Cyanocyclopropyl)-2-fluorophenyl)boronic acid

98%

Reagent Code: #165917
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CAS Number 1256345-50-2

science Other reagents with same CAS 1256345-50-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.99 g/mol
Formula C₁₀H₉BFNO₂
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MDL Number MFCD17926483
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated biaryl compounds. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The presence of fluorine and the cyanocyclopropyl group enhances metabolic stability and binding affinity in drug candidates, particularly in the development of kinase inhibitors and CNS-active agents. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,290.00
inventory 1g
10-20 days ฿12,000.00
inventory 5g
10-20 days ฿53,190.00

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(5-(1-Cyanocyclopropyl)-2-fluorophenyl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated biaryl compounds. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The presence of fluorine and the cyanocyclopropyl group enhances metabolic stability and binding affinity in drug candidates, particularly in the development of kinase inhibitors and CNS-active agents. Commonly employed in

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated biaryl compounds. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The presence of fluorine and the cyanocyclopropyl group enhances metabolic stability and binding affinity in drug candidates, particularly in the development of kinase inhibitors and CNS-active agents. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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