AA20191
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 98% | in stock | $42.00 | $30.00 | - + | |
5g | 95% | in stock | $127.00 | $89.00 | - + | |
25g | 98% | in stock | $511.00 | $358.00 | - + | |
100g | 98% | in stock | $1,505.00 | $1,054.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA20191 |
Chemical Name: | 4-Bromomethyl-3-fluorophenylboronic acid, pinacol ester |
CAS Number: | 1150271-74-1 |
Molecular Formula: | C13H17BBrFO2 |
Molecular Weight: | 314.9863 |
MDL Number: | MFCD11855987 |
SMILES: | BrCc1ccc(cc1F)B1OC(C(O1)(C)C)(C)C |
Complexity: | 295 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 18 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 2 |
2-(4-(Bromomethyl)-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile chemical compound commonly used in organic synthesis. It serves as a valuable building block in the formation of complex organic molecules due to its unique structural properties. This compound is particularly valued for its ability to introduce fluorine and boron functionalities simultaneously into organic frameworks, enabling the creation of novel molecules with diverse applications.In chemical synthesis, 2-(4-(Bromomethyl)-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is often employed as a key reagent in the formation of carbon-carbon and carbon-heteroatom bonds. The bromine and fluorine atoms present in the molecule facilitate efficient cross-coupling reactions with various organic substrates, leading to the generation of complex structures with high precision and selectivity. Furthermore, the boron atom in the dioxaborolane moiety offers a powerful handle for further functionalization, enabling the introduction of additional chemical groups to tailor the properties of the final product.Overall, the strategic incorporation of 2-(4-(Bromomethyl)-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane into synthetic pathways allows chemists to access a wide range of structurally diverse and biologically relevant compounds, making it a valuable tool in the field of chemical synthesis.