AA54596
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $48.00 | $33.00 | - + | |
1g | 97% | in stock | $96.00 | $67.00 | - + | |
5g | 97% | in stock | $362.00 | $253.00 | - + | |
10g | 97% | in stock | $628.00 | $439.00 | - + | |
25g | 97% | in stock | $1,272.00 | $891.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA54596 |
Chemical Name: | 2-Formyl-5-(trifluoromethoxy)phenylboronic acid |
CAS Number: | 1218790-89-6 |
Molecular Formula: | C8H6BF3O4 |
Molecular Weight: | 233.937 |
MDL Number: | MFCD10566600 |
SMILES: | O=Cc1ccc(cc1B(O)O)OC(F)(F)F |
Complexity: | 246 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 7 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 3 |
(2-Formyl-5-(trifluoromethoxy)phenyl)boronic acid is a versatile chemical reagent commonly used in organic synthesis. This compound serves as a key building block in the construction of various biologically active molecules and pharmaceuticals. In chemical synthesis, this boronic acid derivative plays a crucial role as a carbonyl moiety source due to its formyl functional group. By reacting with different nucleophiles or electrophiles, it can participate in a wide range of reactions such as Suzuki coupling, Mannich reaction, and various C-C bond formation processes. The trifluoromethoxy group enhances the reactivity and stability of the compound, making it a valuable tool in modern synthetic organic chemistry.