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(3-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol
For research use only. Not for therapeutic Use.
(3-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol is a boronic ester functionalized phenylmethanol used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its fluorinated phenyl ring and boronate group make it an essential intermediate for producing complex aromatic compounds, including pharmaceuticals and agrochemicals. This compound’s structure allows for precise functionalization, supporting the synthesis of bioactive molecules with enhanced stability and bioavailability. It is widely utilized in medicinal chemistry to facilitate the creation of innovative therapeutic candidates.
Catalog Number | L024308 |
CAS Number | 1400755-06-7 |
Molecular Formula | C13H18BFO3 |
Purity | ≥95% |
IUPAC Name | [3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanol |
InChI | InChI=1S/C13H18BFO3/c1-12(2)13(3,4)18-14(17-12)10-5-9(8-16)6-11(15)7-10/h5-7,16H,8H2,1-4H3 |
InChIKey | PFTKOQBWYWEFTD-UHFFFAOYSA-N |
SMILES | B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC(=C2)F)CO |