Description

[2-Fluoro-4-(4-propylcyclohexyl)phenyl]boronic acid (CAS No. 159119-10-5) is a high-purity boronic acid derivative with the molecular formula C₁₅H₂₂BFO₂. This compound features a fluorinated phenyl ring coupled with a propylcyclohexyl group, making it a valuable intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its unique structure enhances reactivity and selectivity, ideal for constructing complex aromatic systems in pharmaceuticals and advanced materials. The product is supplied as a white to off-white crystalline powder with ≥95% purity (HPLC), ensuring consistent performance in research and industrial applications. Proper storage under inert conditions (2-8°C, argon) is recommended to maintain stability and prevent degradation.

Properties

• CAS Number: 159119-10-5
• Complexity: 267
• IUPAC Name: [2-fluoro-4-(4-propylcyclohexyl)phenyl]boronic acid
• InChI: InChI=1S/C15H22BFO2/c1-2-3-11-4-6-12(7-5-11)13-8-9-14(16(18)19)15(17)10-13/h8-12,18-19H,2-7H2,1H3
• InChI Key: OZKQZVHMAGMWIN-UHFFFAOYSA-N
• Exact Mass: 264.1696883
• Molecular Formula: C15H22BFO2
• Molecular Weight: 264.15
• SMILES: B(C1=C(C=C(C=C1)C2CCC(CC2)CCC)F)(O)O
• Topological: 40.5
• Monoisotopic Mass: 264.1696883
• Synonyms: 159119-10-5, [2-fluoro-4-(4-propylcyclohexyl)phenyl]boronic acid, (2-Fluoro-4-(trans-4-propylcyclohexyl)phenyl)boronic acid, B-[2-fluoro-4-(trans-4-propylcyclohexyl)phenyl]Boronic acid, Boronic acid, B-[2-fluoro-4-(trans-4-propylcyclohexyl)phenyl]-, (2-fluoro-4-(4-propylcyclohexyl)phenyl)boronic acid, {2-fluoro-4-[(1s,4r)-4-propylcyclohexyl]phenyl}boronic acid, 2-Fluoro-4-(trans-4-propylcyclohexyl)phenylboronic acid, SCHEMBL2392780, SCHEMBL6558027, DTXSID301187430, SB67067, 1337992-05-8, DB-064262, DB-215379, [4-(4-Propylcyclohexyl)-2-fluorophenyl]boronicacid, (2-Fluoro-4-(trans-4-propylcyclohexyl)phenyl)boronicacid

Application

This boronic acid derivative is widely used in palladium-catalyzed cross-coupling reactions to synthesize biaryl compounds, a key step in drug discovery and material science. Its fluorinated aromatic ring improves electronic properties, making it suitable for designing liquid crystals and OLED materials. Researchers also employ it in the development of enzyme inhibitors and receptor modulators due to its structural versatility.

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