AA10580
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $22.00 | $15.00 | - + | |
250mg | 95% | in stock | $36.00 | $25.00 | - + | |
1g | 95% | in stock | $59.00 | $42.00 | - + | |
5g | 95% | in stock | $178.00 | $125.00 | - + | |
10g | 95% | in stock | $310.00 | $217.00 | - + | |
25g | 95% | in stock | $691.00 | $484.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA10580 |
Chemical Name: | Potassium (4-methoxy)benzyloxymethyltrifluoroborate |
CAS Number: | 1027642-26-7 |
Molecular Formula: | C9H11BF3KO2 |
Molecular Weight: | 258.0869 |
MDL Number: | MFCD11505925 |
SMILES: | F[B-](COCc1ccc(cc1)OC)(F)F.[K+] |
Complexity: | 184 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 6 |
Rotatable Bond Count: | 4 |
Potassium trifluoro(((4-methoxybenzyl)oxy)methyl)borate is a versatile reagent used in a variety of chemical synthesis applications. Its unique boron-based structure allows for efficient and selective transformations in organic chemistry. When incorporated into reactions, this compound serves as a valuable source of both boron and fluorine functionalities, offering opportunities for the introduction of these elements into organic molecules in a controlled manner.In chemical synthesis, Potassium trifluoro(((4-methoxybenzyl)oxy)methyl)borate is commonly employed as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds. Its use can facilitate reactions such as Suzuki coupling, which enables the cross-coupling of aryl halides or pseudohalides with boronic acids or boronate esters, leading to the synthesis of biaryl compounds. Additionally, this reagent can participate in other key transformations like hydroboration, enabling the selective addition of boron and fluorine groups to alkenes and alkynes.Overall, the application of Potassium trifluoro(((4-methoxybenzyl)oxy)methyl)borate in chemical synthesis demonstrates its importance as a powerful tool for the construction of complex organic molecules with precision and efficiency.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501