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3-Formylphenylboronic acid CAS: 87199-16-4

Short Description:

Catalog Number: XD93443
Cas: 87199-16-4
Molecular Formula: C7H7BO3
Molecular Weight: 149.94
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Product Detail

Product Tags

Catalog Number XD93443
Product Name 3-Formylphenylboronic acid
CAS 87199-16-4
Molecular Formula C7H7BO3
Molecular Weight 149.94
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

3-Formylphenylboronic acid, also known as 3-Formylphenylboronic acid or 3-Benzeneboronic acid, is a chemical compound that has diverse applications in various scientific fields, including organic synthesis, catalysis, and material science.One significant use of 3-Formylphenylboronic acid is as a versatile building block in organic synthesis. The formyl group (CHO) attached to the phenyl ring imparts distinct reactivity to the compound. It can serve as an aldehyde moiety, readily undergoing chemical reactions such as nucleophilic additions, condensations, and transformations into other functional groups. Chemists can take advantage of this reactivity to synthesize a wide range of complex organic molecules.Another important application of 3-Formylphenylboronic acid is in the field of catalysis. Boronic acids, including 3-Formylphenylboronic acid, can act as Lewis acids, which are electron pair acceptors. As such, they can function as catalysts in various transformations, such as C-C bond formation, hydrogenation, and oxidation reactions. The presence of the formyl group in 3-Formylphenylboronic acid enhances its catalytic activity, allowing it to promote specific reactions efficiently.Furthermore, 3-Formylphenylboronic acid is utilized in the development of advanced materials. Boronic acids, with their unique reactivity and ability to form reversible covalent bonds, have been employed in the design and synthesis of smart materials, including polymeric gels, sensors, and bioconjugates. By incorporating 3-Formylphenylboronic acid into the structure of these materials, researchers can achieve desirable properties, such as pH-responsive behavior or selective binding capabilities.In the field of medicinal chemistry, 3-Formylphenylboronic acid can be utilized as a starting material for the synthesis of biologically active compounds. The formyl group can be modified to introduce specific functional groups or pharmacophores, leading to the development of new drug candidates. Boronic acids, including 3-Formylphenylboronic acid derivatives, have shown potential in the treatment of various diseases, such as cancer, diabetes, and inflammation.In summary, 3-Formylphenylboronic acid is a versatile compound with applications in organic synthesis, catalysis, material science, and medicinal chemistry. Its formyl group provides unique reactivity, enabling its use as a building block in the synthesis of complex organic molecules. It can also serve as a catalyst in various reactions. Additionally, it finds utility in the development of advanced materials and as a starting material for medicinal chemistry endeavors. 3-Formylphenylboronic acid contributes to advancements in various scientific disciplines, facilitating the development of new molecules, materials, and therapeutic agents.


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    3-Formylphenylboronic acid CAS: 87199-16-4