3-(4-Fluorophenylformamide) phenylboronic acid

95%

Reagent Code: #44361
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CAS Number 1258236-58-6

science Other reagents with same CAS 1258236-58-6

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Weight 259.0407432 g/mol
Formula C₁₃H₁₁BFNO₃
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorophenyl group can enhance the stability and reactivity of the molecule, making it suitable for creating complex organic structures. It is also explored in medicinal chemistry for designing drug candidates, particularly in targeting enzymes or receptors where the fluorine moiety can improve binding affinity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿23,292.00
inventory 250mg
10-20 days ฿8,802.00
inventory 100mg
10-20 days ฿5,274.00

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3-(4-Fluorophenylformamide) phenylboronic 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 key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorophenyl group can enhance the stability and reactivity of the molecule, making it suitable for crea

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorophenyl group can enhance the stability and reactivity of the molecule, making it suitable for creating complex organic structures. It is also explored in medicinal chemistry for designing drug candidates, particularly in targeting enzymes or receptors where the fluorine moiety can improve binding affinity and metabolic stability.

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