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

95%

Reagent Code: #90530
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CAS Number 2246875-71-6

science Other reagents with same CAS 2246875-71-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.1681232 g/mol
Formula C₁₆H₂₃BFNO₃
badge Registry Numbers
MDL Number MFCD31916410
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active compounds, particularly in the creation of small molecule inhibitors targeting specific enzymes or receptors. Its boronate ester functional group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to form carbon-carbon bonds. This enables the construction of complex molecular structures, which are often explored for their potential therapeutic applications. Additionally, its fluorine substituent can enhance the metabolic stability and binding affinity of the resulting drug candidates, making it a crucial component in the design of novel pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,160.00
inventory 1g
10-20 days ฿52,812.00

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N-(3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)isobutyramide
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This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active compounds, particularly in the creation of small molecule inhibitors targeting specific enzymes or receptors. Its boronate ester functional group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to form carbon-carbon bonds. This enables the construction of complex molecular structures, which are often explored for their potential therapeutic applications. Additionally, its fluorine substituent can enhance the metabolic stability and binding affinity of the resulting drug candidates, making it a crucial component in the design of novel pharmaceuticals.
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