2-(6-([1,1'-Biphenyl]-3-yl)dibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

• CAT Number: L007229
• CAS Number: 1858289-64-1
• Molecular Formula: C30H27BO2S
• Molecular Weight: 462.4
• Purity: ≥95%
• IUPAC Name: 4,4,5,5-tetramethyl-2-[6-(3-phenylphenyl)dibenzothiophen-4-yl]-1,3,2-dioxaborolane
• InChI: InChI=1S/C30H27BO2S/c1-29(2)30(3,4)33-31(32-29)26-18-10-17-25-24-16-9-15-23(27(24)34-28(25)26)22-14-8-13-21(19-22)20-11-6-5-7-12-20/h5-19H,1-4H3
• InChIKey: YIQGVICVAGYGBO-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=C3C(=CC=C2)C4=C(S3)C(=CC=C4)C5=CC=CC(=C5)C6=CC=CC=C6

2-(6-([1,1′-Biphenyl]-3-yl)dibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane（Cat No.:L007229）, is a complex chemical compound utilized in organic synthesis and medicinal chemistry research. Featuring a boron-containing dioxaborolane core, it has potential applications in Suzuki-Miyaura cross-coupling reactions. The biphenyl and dibenzo[b,d]thiophene moieties confer unique reactivity and stability, making them valuable for designing diverse organic molecules. Researchers employ this compound as a key intermediate, enabling the creation of complex structures for drug discovery efforts and advancements in synthetic methodologies, contributing significantly to the field of organic chemistry and pharmaceutical research.