AE25147
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 97% | in stock | $153.00 | $107.00 | - + | |
5g | 97% | in stock | $518.00 | $362.00 | - + | |
10g | 97% | in stock | $875.00 | $612.00 | - + | |
25g | 97% | in stock | $1,707.00 | $1,195.00 | - + | |
100g | 97% | in stock | $5,367.00 | $3,757.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE25147 |
Chemical Name: | 2-(3,4-Bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
CAS Number: | 1073339-08-8 |
Molecular Formula: | C14H15BF6O2 |
Molecular Weight: | 340.0691 |
MDL Number: | MFCD12405522 |
SMILES: | CC1(C)OB(OC1(C)C)c1ccc(c(c1)C(F)(F)F)C(F)(F)F |
Complexity: | 430 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 23 |
Hydrogen Bond Acceptor Count: | 8 |
Rotatable Bond Count: | 1 |
2-(3,4-Bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound widely used in chemical synthesis. This boronic ester serves as a valuable building block in the creation of various organic compounds through Suzuki-Miyaura cross-coupling reactions. Its unique chemical structure, featuring both boron and trifluoromethyl functional groups, imparts advantageous properties that enhance the efficiency and selectivity of these synthetic transformations. By participating in palladium-catalyzed coupling reactions with aryl halides or pseudohalides, this compound facilitates the construction of complex molecular architectures in drug discovery, material science, and agrochemical research.