(5-(((2,4-Dimethoxybenzyl)amino)methyl) -2-fluorophenyl)boronic acid

98%

Reagent Code: #89328
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CAS Number 1704121-14-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.136 g/mol
Formula C₁₆H₁₉BFNO₄
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group makes it a valuable building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its fluorophenyl group can enhance the stability and binding affinity of the resulting molecules, making it useful in medicinal chemistry research.

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inventory 1g
10-20 days ฿50,210.00
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(5-(((2,4-Dimethoxybenzyl)amino)methyl) -2-fluorophenyl)boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group makes it a valuable building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its fluorophenyl group can enhance the

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group makes it a valuable building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its fluorophenyl group can enhance the stability and binding affinity of the resulting molecules, making it useful in medicinal chemistry research.

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