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Chemical Reagents>Organometallic Reagents> 2-Chloro-6-fluoro-3-hydroxyphenylboronic acid pinacol ester
For research use only. Not for therapeutic Use.
2-Chloro-6-fluoro-3-hydroxyphenylboronic acid pinacol ester is an organoboron compound with the formula C12H14BClFHO3. It consists of a phenyl ring substituted with a chloro group at the 2-position, a fluoro group at the 6-position, and a hydroxy group at the 3-position. The boronic acid functionality at the 1-position is esterified with pinacol, a diol compound. This ester is often used in Suzuki coupling reactions in organic synthesis, particularly for the creation of carbon-carbon bonds in drug development and materials science.
| CAS Number | 2121512-89-6 |
| Molecular Formula | C12H15BClFO3 |
| Purity | ≥95% |
| IUPAC Name | 2-chloro-4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol |
| InChI | InChI=1S/C12H15BClFO3/c1-11(2)12(3,4)18-13(17-11)9-7(15)5-6-8(16)10(9)14/h5-6,16H,1-4H3 |
| InChIKey | UHXVCXSLQMMDND-UHFFFAOYSA-N |
| SMILES | B1(OC(C(O1)(C)C)(C)C)C2=C(C=CC(=C2Cl)O)F |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |