2-([1,1':3',1''-Terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

• CAT Number: L029422
• CAS Number: 1115023-84-1
• Molecular Formula: C24H25BO2
• Molecular Weight: 356.30
• Purity: ≥95%
• IUPAC Name: 4,4,5,5-tetramethyl-2-[3-(3-phenylphenyl)phenyl]-1,3,2-dioxaborolane
• InChI: InChI=1S/C24H25BO2/c1-23(2)24(3,4)27-25(26-23)22-15-9-14-21(17-22)20-13-8-12-19(16-20)18-10-6-5-7-11-18/h5-17H,1-4H3
• InChIKey: JVOFKEAEKBTFCW-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC=C2)C3=CC=CC(=C3)C4=CC=CC=C4

2-([1,1′:3′,1”-Terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane（Cat No.:L029422）is a boronic ester compound used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. The molecule features a dioxaborolane group attached to a terphenyl moiety, providing significant reactivity for forming carbon-carbon bonds. The tetramethyl groups add stability to the boronate, making it easier to handle in various chemical reactions. This compound is valuable for creating complex molecular architectures, including pharmaceuticals and advanced materials. Its structure allows for precise functionalization, essential for researchers focused on drug discovery, medicinal chemistry, and material science.