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4-Formylphenylboronic acid CAS: 87199-17-5

Short Description:

Catalog Number: XD93450
Cas: 87199-17-5
Molecular Formula: C7H7BO3
Molecular Weight: 149.94
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Product Detail

Product Tags

Catalog Number XD93450
Product Name 4-Formylphenylboronic acid
CAS 87199-17-5
Molecular Formula C7H7BO3
Molecular Weight 149.94
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

4-Formylphenylboronic acid is an important compound in organic chemistry and finds diverse applications in fields such as pharmaceuticals, materials science, and catalysis. Its chemical structure comprises a boronic acid group attached to a formylphenyl group.One of the significant uses of 4-Formylphenylboronic acid is in the synthesis of pharmaceutical compounds. It can serve as a versatile building block in the construction of biologically active molecules due to its reactivity and ability to form covalent bonds with various functional groups. The formyl group, with its electrophilic nature, allows for the introduction of additional substituents and modifications, which can enhance the desired biological activity or improve drug delivery properties.In materials science, 4-Formylphenylboronic acid can be incorporated into polymers, hydrogels, and other advanced materials to introduce specific functionalities. The boronic acid moiety can participate in reversible covalent bonding with cis-diol groups, such as those present in saccharides or glycoproteins. This property enables the design of stimuli-responsive materials, where changes in pH or glucose concentration can lead to reversible self-assembly, gelation, or changes in material properties. These materials have potential applications in drug delivery, bioimaging, and tissue engineering.Furthermore, 4-Formylphenylboronic acid is utilized as a catalyst in various organic reactions. The boronic acid group can act as a Lewis acid, facilitating reactions such as Lewis acid-catalyzed cycloadditions, condensations, and rearrangements. Its catalytic activity can enhance reaction rates, selectivity, and efficiency in the synthesis of complex organic molecules.Another important application of 4-Formylphenylboronic acid is in the field of sensors and sensing technology. The boronic acid group can selectively bind to certain analytes, such as carbohydrates or catecholamines, forming stable complexes. This property can be utilized to develop sensors for glucose, dopamine, or other important biomolecules. By incorporating this compound into sensor systems, the reversible binding of the boronic acid group can induce changes in fluorescence, conductivity, or electrochemical signals, allowing for sensitive and selective detection.In conclusion, 4-Formylphenylboronic acid is a versatile compound with diverse applications in pharmaceutical synthesis, materials science, catalysis, and sensing technology. Its ability to form reversible covalent bonds, its catalytic activity, and its selectivity for certain analytes make it a valuable tool for researchers in various scientific disciplines. By harnessing the unique properties of 4-Formylphenylboronic acid, scientists can develop novel materials, design biologically active compounds, and fabricate sensitive sensors for a wide range of applications.


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    4-Formylphenylboronic acid CAS: 87199-17-5