3-Fluoro-5-ethoxycarbonylphenylboronic acid
98%
science Other reagents with same CAS 871329-85-0
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group is essential for coupling with aryl halides, making it valuable in pharmaceutical research for developing new drugs and active pharmaceutical ingredients. Additionally, it is employed in material science for creating advanced polymers and organic electronic materials. The fluoro substituent at the 3-position introduces electronic effects that can modulate reactivity and stability, while the ethoxycarbonyl group at the 5-position enhances solubility and reactivity, making it suitable for diverse synthetic applications.
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