Description
2-Benzyloxy-6-fluorophenylboronic acid (CAS No. 1217500-53-2) is a high-purity boronic acid derivative with the molecular formula C13H12BFO3. This compound is a valuable intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for pharmaceutical and materials science applications. Its unique structure, featuring a benzyloxy group and fluorine substitution, enhances reactivity and selectivity in complex transformations. Ideal for researchers and scientists, this product is rigorously tested to ensure >95% purity (HPLC) and is supplied as a white to off-white crystalline powder. Store under inert conditions (2-8°C) to maintain stability. Suitable for use in drug discovery, agrochemical development, and advanced material synthesis.
Properties
- CAS Number: 1217500-53-2
- Complexity: 246
- IUPAC Name: (2-benzyloxy-6-fluoro-phenyl)boronic acid
- InChI: InChI=1S/C13H12BFO3/c15-11-7-4-8-12(13(11)14(16)17)18-9-10-5-2-1-3-6-10/h1-8,16-17H,9H2
- InChI Key: NBRVDQVRGXXXIE-UHFFFAOYSA-N
- Exact Mass: 246.0863526
- Molecular Formula: C13H12BFO3
- Molecular Weight: 246.04
- SMILES: B(C1=C(C=CC=C1F)OCC2=CC=CC=C2)(O)O
- Topological: 49.7
- Monoisotopic Mass: 246.0863526
- Synonyms: 1217500-53-2, 2-Benzyloxy-6-fluorophenylboronic acid, (2-(Benzyloxy)-6-fluorophenyl)boronic acid, (2-fluoro-6-phenylmethoxyphenyl)boronic acid, BORONIC ACID, B-[2-FLUORO-6-(PHENYLMETHOXY)PHENYL]-, MFCD11617256, [2-(Benzyloxy)-6-fluorophenyl]boronic acid, 2-(benzyloxy)-6-fluorophenylboronic acid, (2-Benzyloxy-6-fluoro-phenyl)boronic acid, SCHEMBL18190569, DTXSID40659359, AKOS015839412, s11002, AS-68690, SY034532, (2-(Benzyloxy)-6-fluorophenyl)boronicacid, DB-027822, CS-0095029
2-Benzyloxy-6-fluorophenylboronic acid is widely used in palladium-catalyzed cross-coupling reactions to synthesize biaryl compounds for pharmaceutical intermediates. Its fluorine moiety enhances metabolic stability in drug candidates, making it valuable in medicinal chemistry. The compound also serves as a building block in OLED materials and ligand design for catalysis. Handle under inert conditions to prevent boronic acid degradation.
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