Atomfair (4′-Butyl-[1,1′-biphenyl]-4-yl)boronic acid C16H19BO2 CAS 145413-17-8

Description

(4′-Butyl-[1,1′-biphenyl]-4-yl)boronic acid (CAS No. 145413-17-8) is a high-purity boronic acid derivative with the molecular formula C₁₆H₁₉BO₂. This compound features a biphenyl core substituted with a butyl group at the 4′-position and a boronic acid moiety at the 4-position, making it a versatile intermediate in organic synthesis and cross-coupling reactions. Its well-defined structure ensures excellent reactivity in Suzuki-Miyaura couplings, a cornerstone of modern pharmaceutical and materials science research. Suitable for use in both academic and industrial settings, this product is rigorously tested for purity and stability, ensuring reliable performance in your experiments. Available in various quantities to meet your research needs.

Properties

• CAS Number: 145413-17-8
• Complexity: 241
• IUPAC Name: [4-(4-butylphenyl)phenyl]boronic acid
• InChI: InChI=1S/C16H19BO2/c1-2-3-4-13-5-7-14(8-6-13)15-9-11-16(12-10-15)17(18)19/h5-12,18-19H,2-4H2,1H3
• InChI Key: DKCMBSJGEAEGOE-UHFFFAOYSA-N
• Exact Mass: 254.1478100
• Molecular Formula: C16H19BO2
• Molecular Weight: 254.1
• SMILES: B(C1=CC=C(C=C1)C2=CC=C(C=C2)CCCC)(O)O
• Topological: 40.5
• Monoisotopic Mass: 254.1478100
• Synonyms: 145413-17-8, (4′-Butyl-[1,1′-biphenyl]-4-yl)boronic acid, [4-(4-butylphenyl)phenyl]boronic acid, Boronic acid, B-(4′-butyl[1,1′-biphenyl]-4-yl)-, (4′-Butyl[1,1′-biphenyl]-4-yl)-boronic acid, {4′-butyl-[1,1′-biphenyl]-4-yl}boronic acid, 4′-butylbiphenyl-4-ylboronic acid, 4′-Butyl-4-biphenylboronic acid, (4′-Butyl[1,1′-biphenyl]-4-yl)boronic acid, SCHEMBL13454827, 4′-butylbiphenyl-4-boronic acid, DTXSID60678921, MFCD08275638, AKOS005146021, SB66791, DB-024677, (4′-Butyl-[1,1′-biphenyl]-4-yl)boronicacid, B-(4′-butyl[1,1′-biphenyl]-4-yl)boronic acid, (4/’-Butyl[1,1/’-biphenyl]-4-yl)-boronic acid

Application

(4′-Butyl-[1,1′-biphenyl]-4-yl)boronic acid is widely used as a key building block in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds. It finds applications in pharmaceutical research, particularly in the development of novel drug candidates and bioactive molecules. Additionally, this boronic acid derivative is employed in materials science for the preparation of advanced organic electronic materials and liquid crystals. Its stability and reactivity make it a preferred choice for researchers working on complex organic transformations.

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