4-Cyano-2-fluorophenylboronic Acid

98%

Reagent Code: #163981
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CAS Number 1150114-77-4

science Other reagents with same CAS 1150114-77-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.932 g/mol
Formula C₇H₅BFNO₂
badge Registry Numbers
MDL Number MFCD07644472
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds for pharmaceutical and agrochemical intermediates. Its boronic acid group enables efficient coupling with aryl halides, while the cyano and fluoro substituents provide sites for further functionalization or influence electronic properties in target molecules. Commonly employed in the development of bioactive compounds and functional materials.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,230.00
inventory 5g
10-20 days ฿31,900.00
inventory 10g
10-20 days ฿60,190.00
inventory 1g
10-20 days ฿9,100.00

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4-Cyano-2-fluorophenylboronic Acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds for pharmaceutical and agrochemical intermediates. Its boronic acid group enables efficient coupling with aryl halides, while the cyano and fluoro substituents provide sites for further functionalization or influence electronic properties in target molecules. Commonly employed in the development of bioactive compounds and functional materials.

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds for pharmaceutical and agrochemical intermediates. Its boronic acid group enables efficient coupling with aryl halides, while the cyano and fluoro substituents provide sites for further functionalization or influence electronic properties in target molecules. Commonly employed in the development of bioactive compounds and functional materials.

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