Description

(6-Phenyldibenzo[b,d]furan-4-yl)boronic acid (CAS No. 1010068-85-5) is a high-purity boronic acid derivative with the molecular formula C₁₈H₁₃BO₃. This compound features a dibenzofuran core functionalized with a phenyl group at the 6-position and a boronic acid moiety at the 4-position, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions and other transition-metal-catalyzed transformations. Its rigid aromatic structure and boronic acid functionality enable precise molecular design in organic synthesis, pharmaceuticals, and materials science. Ideal for researchers and scientists, this product is supplied with comprehensive analytical data (including ¹H NMR, ¹³C NMR, and HPLC) to ensure quality and reproducibility. Store under inert conditions to maintain stability.

Properties

• CAS Number: 1010068-85-5
• Complexity: 383
• IUPAC Name: (6-phenyldibenzofuran-4-yl)boronic acid
• InChI: InChI=1S/C18H13BO3/c20-19(21)16-11-5-10-15-14-9-4-8-13(17(14)22-18(15)16)12-6-2-1-3-7-12/h1-11,20-21H
• InChI Key: UYZXLKMREZFZPU-UHFFFAOYSA-N
• Exact Mass: 288.0957744
• Molecular Formula: C18H13BO3
• Molecular Weight: 288.1
• SMILES: B(C1=C2C(=CC=C1)C3=C(O2)C(=CC=C3)C4=CC=CC=C4)(O)O
• Topological: 53.6
• Monoisotopic Mass: 288.0957744
• Synonyms: 1010068-85-5, (6-Phenyldibenzo[b,d]furan-4-yl)boronic acid, Boronic acid, B-(6-phenyl-4-dibenzofuranyl)-, B-(6-phenyl-4-dibenzofuranyl)-Boronic acid, (6-phenyldibenzofuran-4-yl)boronic acid, MFCD29077673, {10-phenyl-8-oxatricyclo[7.4.0.0(2),?]trideca-1(9),2(7),3,5,10,12-hexaen-6-yl}boronic acid, SCHEMBL14935848, UYZXLKMREZFZPU-UHFFFAOYSA-N, DTXSID001269396, CS-B1242, 6-Phenyldibenzofuran-4-boronic Acid, AKOS027430370, AS-55775, SY273337, B-(6-Phenyl-4-dibenzofuranyl)-boronicacid, B-(6-Phenyl-4-dibenzofuranyl)boronic acid, Phenyldibenzo[b,d]furan-4-yl)boronic acid, DB-213556, (6-Phenyldibenzo[b,d]furan-4-yl)boronicacid, A11819, BDPFR-B; (6-phenyldibenzo[b,d]furan-4-yl)boronic acid, (6-Phenyldibenzo[b,d]furan-4-yl)boronic acid(Contains varying amounts of anhydride), {10-phenyl-8-oxatricyclo[7.4.0.0?,?]trideca-1(9),2(7),3,5,10,12-hexaen-6-yl}boronic acid

Application

(6-Phenyldibenzo[b,d]furan-4-yl)boronic acid is widely used in pharmaceutical research as a key intermediate for synthesizing bioactive molecules and heterocyclic compounds. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex biaryl structures for drug discovery. The compound’s dibenzofuran scaffold also makes it valuable in materials science, particularly in the development of organic semiconductors and luminescent materials.

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