1-(3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxylic acid

97%

Reagent Code: #128797
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CAS Number 2096998-21-7

science Other reagents with same CAS 2096998-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.14 g/mol
Formula C₁₆H₂₀BFO₄
badge Registry Numbers
MDL Number MFCD22192535
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester functionality enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive compounds and functional materials. The cyclopropane carboxylic acid moiety can serve as a structural motif to enhance metabolic stability and influence conformation in drug design. Commonly employed in late-stage functionalization due to its compatibility with palladium-catalyzed transformations.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,210.00
inventory 100mg
10-20 days ฿12,240.00
inventory 250mg
10-20 days ฿21,430.00
inventory 1g
10-20 days ฿49,320.00

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1-(3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxylic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester functionality enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive compounds and functional materials. The cyclopropane carboxylic acid moiety can serve as a structural motif to enhance metabolic stability and influence conformation in drug design. Commonly employed in

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester functionality enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive compounds and functional materials. The cyclopropane carboxylic acid moiety can serve as a structural motif to enhance metabolic stability and influence conformation in drug design. Commonly employed in late-stage functionalization due to its compatibility with palladium-catalyzed transformations.

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