2-Formylfuran-5-boronic acid CAS: 27329-70-0
Catalog Number | XD93448 |
Product Name | 2-Formylfuran-5-boronic acid |
CAS | 27329-70-0 |
Molecular Formula | C5H5BO4 |
Molecular Weight | 139.9 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2-Formylfuran-5-boronic acid is an organic compound that has gained significance in the field of organic synthesis, medicinal chemistry, and materials science. It is a boronic acid derivative of furan containing a formyl group (-CHO) at the 2-position. This unique chemical structure provides it with several useful applications.One of the primary applications of 2-Formylfuran-5-boronic acid lies in its ability to serve as a reagent in palladium-catalyzed cross-coupling reactions. It can participate in Suzuki-Miyaura or Heck reactions, where it acts as the boron source to form carbon-carbon bonds with aryl or vinyl halides. These reactions are widely utilized in synthetic chemistry to construct complex organic molecules and functionalized heterocycles. By employing 2-Formylfuran-5-boronic acid as a coupling partner, chemists can introduce the furan moiety into target compounds, which can confer desired properties or reactivity.The formyl group in 2-Formylfuran-5-boronic acid also makes it a valuable building block for the synthesis of bioactive compounds. The aldehyde functionality enables various chemical transformations, such as condensation or reduction reactions. These reactions can be employed to modify the structure of 2-Formylfuran-5-boronic acid or to introduce it into more complex molecules. The resulting compounds can exhibit diverse biological activities and can be explored for the development of pharmaceuticals or agrochemicals. For example, furan derivatives have shown potential as antitumor, antimicrobial, and anti-inflammatory agents.Moreover, 2-Formylfuran-5-boronic acid can be utilized in materials science for the preparation of functional materials and surface modifications. Its boronic acid group allows for the formation of reversible covalent bonds with diols or hydroxyl-containing compounds. This property can be exploited to create responsive materials or coatings, where the structural or chemical properties can be dynamically controlled or altered. Additionally, the furan ring can participate in polymerization reactions, leading to the synthesis of furan-based polymers or copolymers with tailored properties. These materials can find applications in areas such as drug delivery, sensors, and electronics.In summary, 2-Formylfuran-5-boronic acid is a versatile compound with diverse applications in organic synthesis, medicinal chemistry, and materials science. Its ability to undergo palladium-catalyzed cross-coupling reactions, its usefulness as a building block for bioactive compounds, and its role in the development of functional materials make it an important tool for researchers working in various scientific disciplines.