(4-Fluoro-3-(isopropylcarbamoyl)phenyl)boronic acid

98%

Reagent Code: #131052
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CAS Number 874219-21-3

science Other reagents with same CAS 874219-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.03 g/mol
Formula C₁₀H₁₃BFNO₃
badge Registry Numbers
MDL Number MFCD08235040
thermostat Physical Properties
Melting Point 263-265 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical research. Serves as a key intermediate in developing protease inhibitors and other bioactive molecules. Its boronic acid group enables selective binding to diols, making it useful in sensor design and targeted drug delivery systems. Also applied in the preparation of covalent inhibitors due to enhanced reactivity and stability imparted by the fluorophenyl and isopropylcarbamoyl groups.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿4,510.00
250mg
10-20 days ฿1,950.00
(4-Fluoro-3-(isopropylcarbamoyl)phenyl)boronic acid
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Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical research. Serves as a key intermediate in developing protease inhibitors and other bioactive molecules. Its boronic acid group enables selective binding to diols, making it useful in sensor design and targeted drug delivery systems. Also applied in the preparation of covalent inhibitors due to enhanced reactivity and stability imparted by the fluorophenyl and isopropylcarbamoyl groups.

Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical research. Serves as a key intermediate in developing protease inhibitors and other bioactive molecules. Its boronic acid group enables selective binding to diols, making it useful in sensor design and targeted drug delivery systems. Also applied in the preparation of covalent inhibitors due to enhanced reactivity and stability imparted by the fluorophenyl and isopropylcarbamoyl groups.

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