(4-(Diethylcarbamoyl)-3-fluorophenyl)boronic acid
98%
Reagent
Code: #90528
CAS Number
874289-14-2
blur_circular Chemical Specifications
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Molecular Information
Weight
239.05 g/mol
Formula
C₁₁H₁₅BFNO₃
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Registry Numbers
MDL Number
MFCD08436057
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Physical Properties
Melting Point
158-160°C
Boiling Point
433.3°C
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Storage & Handling
Density
1.21g/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. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, the presence of the diethylcarbamoyl and fluorine groups can enhance its reactivity and selectivity in specific reactions, contributing to the development of novel compounds with potential applications in drug discovery and advanced materials.
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(4-(Diethylcarbamoyl)-3-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, the presence of the diethylcarbamoyl and fluorine groups can enhance its reactivity and selectivity in specific reactions, contributing to the development of novel compounds with potential applications in drug discovery and advanced materials.
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