[3-[(2-fluorophenyl)carbamoyl]phenyl]boronic acid

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Reagent Code: #89093
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CAS Number 874288-35-4

science Other reagents with same CAS 874288-35-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.04 g/mol
Formula C₁₃H₁₁BFNO₃
badge Registry Numbers
MDL Number MFCD09027208
inventory_2 Storage & Handling
Density 1.34g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of biologically active compounds, especially those targeting neurological and inflammatory disorders. Its fluorophenyl group enhances its binding affinity in certain drug-receptor interactions, contributing to its effectiveness in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,600.00
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[3-[(2-fluorophenyl)carbamoyl]phenyl]boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of biologically active compounds, especially those targeting neurological and inflammatory disorders. Its fluorophenyl group enhances its b

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the synthesis of biologically active compounds, especially those targeting neurological and inflammatory disorders. Its fluorophenyl group enhances its binding affinity in certain drug-receptor interactions, contributing to its effectiveness in medicinal chemistry.

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