(4-(Dimethylcarbamoyl)-2-fluorophenyl)boronic acid

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Reagent Code: #90749
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CAS Number 874289-30-2

science Other reagents with same CAS 874289-30-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.99 g/mol
Formula C₉H₁₁BFNO₃
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MDL Number MFCD11855833
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. Its structure, featuring a dimethylcarbamoyl group and a fluorine substituent, makes it a valuable building block for creating complex molecules, especially in pharmaceutical research. The fluorine atom can enhance the binding affinity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, the boronic acid moiety facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures, which are common in many active pharmaceutical ingredients. Its application extends to materials science, where it can be used to modify polymers or create advanced organic materials with specific properties.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿4,113.00
inventory 1g
10-20 days ฿11,700.00

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(4-(Dimethylcarbamoyl)-2-fluorophenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. Its structure, featuring a dimethylcarbamoyl group and a fluorine substituent, makes it a valuable building block for creating complex molecules, especially in pharmaceutical research. The fluorine atom can enhance the binding affinity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, the boronic aci

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. Its structure, featuring a dimethylcarbamoyl group and a fluorine substituent, makes it a valuable building block for creating complex molecules, especially in pharmaceutical research. The fluorine atom can enhance the binding affinity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, the boronic acid moiety facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures, which are common in many active pharmaceutical ingredients. Its application extends to materials science, where it can be used to modify polymers or create advanced organic materials with specific properties.

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