3-Fluoro-5-(diethylcarbamoyl)phenylboronic acid

98%

Reagent Code: #90168
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CAS Number 871332-64-8
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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.05 g/mol
Formula C₁₁H₁₅BFNO₃
badge Registry Numbers
MDL Number MFCD07363794
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of enzyme inhibitors and receptor modulators. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable for constructing complex molecules in drug discovery. Additionally, it is employed in the preparation of bioactive compounds targeting neurological disorders due to its unique structural properties. The fluorine atom enhances metabolic stability and binding affinity, making it a preferred choice in medicinal chemistry research.

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Test Parameter Specification
APPEARANCE white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,600.00
inventory 500mg
10-20 days ฿24,000.00

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3-Fluoro-5-(diethylcarbamoyl)phenylboronic acid
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Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of enzyme inhibitors and receptor modulators. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable for constructing complex molecules in drug discovery. Additionally, it is employed in the preparation of bioactive compounds targeting neurological disorders due to its unique structural properties. The fluorine atom enhances metaboli

Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of enzyme inhibitors and receptor modulators. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable for constructing complex molecules in drug discovery. Additionally, it is employed in the preparation of bioactive compounds targeting neurological disorders due to its unique structural properties. The fluorine atom enhances metabolic stability and binding affinity, making it a preferred choice in medicinal chemistry research.

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