Description
4,4,5,5-Tetramethyl-2-(9-phenyldibenzo[b,d]furan-3-yl)-1,3,2-dioxaborolane (CAS: 2360830-98-2) is a high-purity boronate ester compound with the molecular formula C24H23BO3. This advanced organic intermediate features a dibenzofuran core functionalized with a phenyl group and a 4,4,5,5-tetramethyl-1,3,2-dioxaborolane moiety, making it an ideal reagent for Suzuki-Miyaura cross-coupling reactions and other transition-metal-catalyzed transformations. With exceptional stability and reactivity, this compound is rigorously tested to meet the stringent requirements of pharmaceutical research, materials science, and organic synthesis applications. Offered in various packaging options under inert atmosphere to ensure long-term stability and performance consistency.
Properties
- CAS Number: 2360830-98-2
- Complexity: 554
- IUPAC Name: 4,4,5,5-tetramethyl-2-(9-phenyldibenzofuran-3-yl)-1,3,2-dioxaborolane
- InChI: InChI=1S/C24H23BO3/c1-23(2)24(3,4)28-25(27-23)17-13-14-19-21(15-17)26-20-12-8-11-18(22(19)20)16-9-6-5-7-10-16/h5-15H,1-4H3
- InChI Key: QCZRKWZKCZOQHJ-UHFFFAOYSA-N
- Exact Mass: 370.1740248
- Molecular Formula: C24H23BO3
- Molecular Weight: 370.2
- SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)C4=C(C=CC=C4O3)C5=CC=CC=C5
- Topological: 31.6
- Monoisotopic Mass: 370.1740248
- Synonyms: 4,4,5,5-Tetramethyl-2-(9-phenyldibenzo[b,d]furan-3-yl)-1,3,2-dioxaborolane, 2360830-98-2, starbld0015670, SCHEMBL21109824, MFCD34698257, G65322, 1-Phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)dibenzofuran
Application
This boronate ester is widely used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and materials science research. It serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions to create biaryl structures. The compound’s stability and reactivity make it valuable for developing advanced OLED materials and π-conjugated systems. Researchers also utilize it in the preparation of novel ligands for catalytic applications.
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