(2,6-Difluoro-4-isopropoxyphenyl)boronic acid

97%

Reagent Code: #178483
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CAS Number 2096337-66-3

science Other reagents with same CAS 2096337-66-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.99 g/mol
Formula C₉H₁₁BF₂O₃
badge Registry Numbers
MDL Number MFCD22689791
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl halides, making it valuable for constructing biaryl structures found in bioactive compounds. The fluorine and isopropoxy substituents enhance electronic and steric properties, improving selectivity and stability in target molecules. Commonly employed in the development of fluorinated drugs and functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿660.00
inventory 250mg
10-20 days ฿1,420.00
inventory 1g
10-20 days ฿4,240.00
inventory 5g
10-20 days ฿21,170.00

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(2,6-Difluoro-4-isopropoxyphenyl)boronic acid
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Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl halides, making it valuable for constructing biaryl structures found in bioactive compounds. The fluorine and isopropoxy substituents enhance electronic and steric properties, improving selectivity and stability in target molecules. Commonly employed in the development of fluorinat

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl halides, making it valuable for constructing biaryl structures found in bioactive compounds. The fluorine and isopropoxy substituents enhance electronic and steric properties, improving selectivity and stability in target molecules. Commonly employed in the development of fluorinated drugs and functional materials.

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