Description

(3-Fluoro-4′-propyl-[1,1′-biphenyl]-4-yl)boronic acid (CAS No. 909709-42-8) is a high-purity boronic acid derivative with the molecular formula C₁₅H₁₆BFO₂. This compound, also known by its IUPAC name [2-fluoro-4-(4-propylphenyl)phenyl]boronic acid, is a valuable building block in organic synthesis and pharmaceutical research. It features a biphenyl scaffold substituted with a fluorine atom and a propyl group, enhancing its reactivity and selectivity in cross-coupling reactions such as Suzuki-Miyaura couplings. The boronic acid moiety enables efficient formation of carbon-carbon bonds, making it indispensable for constructing complex molecular architectures. This product is rigorously tested for quality, ensuring optimal performance in research and industrial applications. Available in various quantities, it is supplied with detailed analytical data including ¹H NMR, ¹³C NMR, and HPLC purity reports.

Properties

• CAS Number: 909709-42-8
• Complexity: 267
• IUPAC Name: [2-fluoro-4-(4-propylphenyl)phenyl]boronic acid
• InChI: InChI=1S/C15H16BFO2/c1-2-3-11-4-6-12(7-5-11)13-8-9-14(16(18)19)15(17)10-13/h4-10,18-19H,2-3H2,1H3
• InChI Key: XZGCBSYWWZAXRC-UHFFFAOYSA-N
• Exact Mass: 258.1227381
• Molecular Formula: C15H16BFO2
• Molecular Weight: 258.10
• SMILES: B(C1=C(C=C(C=C1)C2=CC=C(C=C2)CCC)F)(O)O
• Topological: 40.5
• Monoisotopic Mass: 258.1227381
• Synonyms: 909709-42-8, (3-Fluoro-4′-propyl-[1,1′-biphenyl]-4-yl)boronic acid, 4”-PROPYL-3-FLUOROBIPHENYL-4-BORONIC ACID, 4′-PROPYL-3-FLUOROBIPHENYL-4-BORONIC ACID, 4′-Propyl-3-fluoro-biphenyl-4-boronic acid, [2-fluoro-4-(4-propylphenyl)phenyl]boronic acid, 3-Fluoro-4′-propyl-4-biphenylboronic Acid, 4′-Propyl-3-fluoro-4-biphenyl boronic acid, MFCD10687198, 4′-Propyl-3-fluoro-4-biphenyl boronic acid, {3-fluoro-4′-propyl-[1,1′-biphenyl]-4-yl}boronic acid, C15H16BFO2, Boronic acid, (3-fluoro-4′-propyl[1,1′-biphenyl]-4-yl)-, SCHEMBL1533780, (3-Fluoro-4′-propyl[1,1′-biphenyl]-4-yl)boronic acid, DTXSID90695025, AKOS016003079, GS-6335, SB66948, 3-Fluoro-4′-n-propylbiphenyl-4-boronic, SY055287, 4′-propyl-3-fluoro-4-biphenylboronic acid, DB-078848, 3-fluoro-4′-propylbiphenyl-4-ylboronic acid, CS-0152418, F0942, 2-fluoro-4-(4-propylphenyl)phenylboronic acid, 4-Propyl-3′-Fluorobiphenyl-4′-Boronic Acid, 3-Fluoro-4 inverted exclamation mark -propylbiphenyl-4-boronic Acid, 3-Fluoro-4′-propyl-4-biphenylboronic Acid (contains varying amounts of Anhydride)

Application

(3-Fluoro-4′-propyl-[1,1′-biphenyl]-4-yl)boronic acid is widely used in pharmaceutical and materials science research as a key intermediate in Suzuki-Miyaura cross-coupling reactions. Its unique structure facilitates the synthesis of biaryl compounds, which are prevalent in drug discovery and liquid crystal materials. The fluorine substituent enhances metabolic stability and binding affinity in bioactive molecules. Researchers also utilize this boronic acid derivative in the development of advanced organic electronic materials. Its high reactivity and selectivity make it a preferred choice for constructing complex organic frameworks.

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