N-(4-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzamide

95%

Reagent Code: #84079
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CAS Number 2246760-60-9

science Other reagents with same CAS 2246760-60-9

blur_circular Chemical Specifications

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Weight 341.184 g/mol
Formula C₁₉H₂₁BFNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, which is essential for creating carbon-carbon bonds in pharmaceutical and materials research. Its boronate ester group acts as a key intermediate, enabling the formation of complex organic molecules. It is also employed in the development of biologically active compounds, including potential drug candidates, due to its ability to introduce fluorine atoms into aromatic systems, which can enhance metabolic stability and binding affinity. Additionally, it finds use in the preparation of advanced materials, such as organic semiconductors and polymers, where precise molecular architecture is critical.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿5,778.00
inventory 100mg
10-20 days ฿17,280.00

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N-(4-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzamide
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, which is essential for creating carbon-carbon bonds in pharmaceutical and materials research. Its boronate ester group acts as a key intermediate, enabling the formation of complex organic molecules. It is also employed in the development of biologically active compounds, including potential drug candidates, due to its ability to introduce fluorine atoms into aromatic systems,

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, which is essential for creating carbon-carbon bonds in pharmaceutical and materials research. Its boronate ester group acts as a key intermediate, enabling the formation of complex organic molecules. It is also employed in the development of biologically active compounds, including potential drug candidates, due to its ability to introduce fluorine atoms into aromatic systems, which can enhance metabolic stability and binding affinity. Additionally, it finds use in the preparation of advanced materials, such as organic semiconductors and polymers, where precise molecular architecture is critical.

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