(5-(Benzylcarbamoyl)-2-fluorophenyl)boronic acid
98%
Reagent
Code: #89346
CAS Number
874289-53-9
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Molecular Information
Weight
273.07 g/mol
Formula
C₁₄H₁₃BFNO₃
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Registry Numbers
MDL Number
MFCD08436031
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Physical Properties
Melting Point
224-226 °C
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Storage & Handling
Storage
room temperature, inert gas storage
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals and complex organic molecules. Its fluorophenyl group enhances its reactivity and selectivity in these reactions, making it valuable for constructing biologically active compounds. Additionally, it is employed in the preparation of intermediates for drug discovery, especially in targeting specific enzymes or receptors. Its benzylcarbamoyl moiety can also contribute to the stability and solubility of the resulting compounds, aiding in their application in medicinal chemistry.
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(5-(Benzylcarbamoyl)-2-fluorophenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals and complex organic molecules. Its fluorophenyl group enhances its reactivity and selectivity in these reactions, making it valuable for constructing biologically active compounds. Additionally, it is employed in the preparation of intermediates for drug discovery, especially in targeting specific enzymes or receptors. Its benzylcarbamoyl moiety can also contribute to the stability and solubility of the resulting compounds, aiding in their application in medicinal chemistry.
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