BJ57161
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | 1 week | $49.00 | $35.00 | - + | |
1g | 97% | 1 week | $131.00 | $92.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | BJ57161 |
Chemical Name: | 4-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]dibenzofuran |
CAS Number: | 1056113-44-0 |
Molecular Formula: | C24H23BO3 |
Molecular Weight: | 370.2486 |
MDL Number: | MFCD06434734 |
SMILES: | CC1(C)OB(OC1(C)C)c1ccc(cc1)c1cccc2c1oc1c2cccc1 |
4-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]dibenzofuran is a versatile compound widely used in chemical synthesis. This specific molecule serves as a key building block in the creation of complex organic structures and functional materials. Its unique molecular structure allows for precise control over the positioning of boron atoms, enabling strategic and selective reactions in various synthesis processes.In chemical synthesis, 4-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]dibenzofuran plays a crucial role as a boron-containing reagent. The boron group attached to the molecule serves as a valuable handle for further functionalization through Suzuki-Miyaura cross-coupling reactions. This method allows for the formation of new carbon-carbon bonds under mild conditions, facilitating the construction of complex molecular architectures with high efficiency and precision.Moreover, the dibenzofuran moiety in this compound imparts significant aromatic and electron-rich properties, making it a valuable component in the design of organic semiconductors, optoelectronic materials, and pharmaceutical intermediates. By harnessing the unique reactivity and structural features of 4-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]dibenzofuran, chemists can further explore its potential in the synthesis of advanced materials and bioactive compounds, paving the way for innovative research and development in the field of organic chemistry.