[4-(dimethylcarbamoyl)-3-fluorophenyl]boronic acid
98%
Reagent
Code: #90532
CAS Number
874289-13-1
blur_circular Chemical Specifications
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Molecular Information
Weight
211 g/mol
Formula
C₉H₁₁BFNO₃
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Registry Numbers
MDL Number
MFCD08436060
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Physical Properties
Melting Point
147-149°C
Boiling Point
418.8°C
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Storage & Handling
Density
1.28g/mL
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The dimethylcarbamoyl and fluorine substituents enhance its reactivity and selectivity, allowing for precise modifications in complex molecular structures. It is also employed in the development of bioactive molecules and as a building block in medicinal chemistry for designing potential drug candidates. Additionally, its stability and compatibility with various reaction conditions make it a versatile reagent in research and industrial applications.
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[4-(dimethylcarbamoyl)-3-fluorophenyl]boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The dimethylcarbamoyl and fluorine substituents enhance its reactivity and selectivity, allowing for precise modifications in complex molecular structures. It is also employed in the development of bioactive molecules and as a building block in medicinal chemistry for designing potential drug candidates. Additionally, its stability and compatibility with various reaction conditions make it a versatile reagent in research and industrial applications.
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