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(1-Ethyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)boronic acid
For research use only. Not for therapeutic Use.
(1-Ethyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)boronic Acid(Cat No.:L028346)is a specialized boronic acid derivative crucial for cross-coupling reactions in organic synthesis. The pyrazole ring, enriched with a trifluoromethyl group at the 3-position, enhances the electron-withdrawing characteristics, improving its reactivity and stability. The ethyl group at the 1-position adds lipophilic balance, aiding in solubility and processability. The boronic acid functionality at the 4-position is key for Suzuki-Miyaura coupling, allowing the formation of biaryl compounds essential in pharmaceuticals and agrochemicals, thereby facilitating the creation of diverse and complex molecular architectures.
Catalog Number | L028346 |
CAS Number | 2287228-20-8 |
Molecular Formula | C6H8BF3N2O2 |
Purity | ≥95% |
IUPAC Name | [1-ethyl-3-(trifluoromethyl)pyrazol-4-yl]boronic acid |
InChI | InChI=1S/C6H8BF3N2O2/c1-2-12-3-4(7(13)14)5(11-12)6(8,9)10/h3,13-14H,2H2,1H3 |
InChIKey | ONQLQTCDZMHNEU-UHFFFAOYSA-N |
SMILES | B(C1=CN(N=C1C(F)(F)F)CC)(O)O |