(4-Carbamoyl-2-fluorophenyl)boronic acid
98%
Reagent
Code: #90617
CAS Number
874289-22-2
blur_circular Chemical Specifications
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Molecular Information
Weight
182.94 g/mol
Formula
C₇H₇BFNO₃
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Registry Numbers
MDL Number
MFCD09800867
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Physical Properties
Boiling Point
359.8°C
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Storage & Handling
Density
1.41g/mL
Storage
2-8°C
description Product Description
(4-Carbamoyl-2-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the formation of complex organic molecules. Additionally, it is utilized in the development of bioactive compounds and drug candidates due to its ability to interact with biological targets. Its fluorophenyl moiety further enhances its utility in creating compounds with specific electronic and steric properties.
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(4-Carbamoyl-2-fluorophenyl)boronic acid
(4-Carbamoyl-2-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the formation of complex organic molecules. Additionally, it is utilized in the development of bioactive compounds and drug candidates due to its ability to interact with biological targets. Its fluorophenyl moiety further enhances its utility in creating compounds with specific electronic and steric properties.
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