Description

(2′-Bromo-[1,1′-biphenyl]-2-yl)boronic acid (CAS: 1089189-34-3) is a high-purity boronic acid derivative with the molecular formula C₁₂H₁₀BBrO₂. This compound is a versatile building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and material science applications. Its biphenyl backbone and bromo substituent enhance reactivity and selectivity, making it invaluable for researchers developing novel compounds. Available in ≥95% purity, this product is rigorously tested via HPLC, NMR, and mass spectrometry to ensure consistency and performance. Suitable for use under inert conditions due to its sensitivity to moisture and oxygen.

Properties

• CAS Number: 1089189-34-3
• Complexity: 225
• IUPAC Name: [2-(2-bromophenyl)phenyl]boronic acid
• InChI: InChI=1S/C12H10BBrO2/c14-12-8-4-2-6-10(12)9-5-1-3-7-11(9)13(15)16/h1-8,15-16H
• InChI Key: BXYVFENPSFGAIM-UHFFFAOYSA-N
• Exact Mass: 275.99572
• Molecular Formula: C12H10BBrO2
• Molecular Weight: 276.92
• SMILES: B(C1=CC=CC=C1C2=CC=CC=C2Br)(O)O
• Topological: 40.5
• Monoisotopic Mass: 275.99572
• Synonyms: (2′-bromo-[1,1′-biphenyl]-2-yl)boronic acid, 1089189-34-3, [2-(2-bromophenyl)phenyl]boronic acid, SCHEMBL17969645, BXYVFENPSFGAIM-UHFFFAOYSA-N, 2′-Bromobiphenyl-2-ylboronic acid, MFCD25973301, IMidazo[1,2-a]pyridine, 5-chloro-8-iodo-, (2′-bromo-[1,1′-biphenyl]-2-yl)boronicacid, F75957, (2”-Bromo-[1,1”-biphenyl]-2-yl)boronic Acid

(2′-Bromo-[1,1′-biphenyl]-2-yl)boronic acid is widely used in palladium-catalyzed cross-coupling reactions to synthesize biaryl structures, key intermediates in drug discovery. It serves as a precursor for functionalized biphenyls in materials science, such as OLEDs and liquid crystals. Researchers also employ it in PROTAC development and kinase inhibitor design due to its robust reactivity.

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