(4-[(4-Fluorophenyl)Methyl]CarbamoylPhenyl)Boronic Acid
95%
Reagent
Code: #90458
CAS Number
874460-12-5
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Molecular Information
Weight
273.067 g/mol
Formula
C₁₄H₁₃BFNO₃
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Registry Numbers
MDL Number
MFCD31648851
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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 key intermediate for forming carbon-carbon bonds. Its boronic acid functional 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 fluorine-substituted aromatic ring enhances its reactivity and selectivity in these reactions, making it suitable for constructing complex molecular 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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(4-[(4-Fluorophenyl)Methyl]CarbamoylPhenyl)Boronic Acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for forming carbon-carbon bonds. Its boronic acid functional 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 fluorine-substituted aromatic ring enhances its reactivity and selectivity in these reactions, making it suitable for constructing complex molecular 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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