9,9-Dioctylfluorene-2,7-diboronic Acid bis(Pinacol) Ester

• CAT Number: R015001
• CAS Number: 196207-58-6
• Molecular Formula: C41H64B2O4
• Molecular Weight: 642.57
• Purity: ≥95%
• Synonyms: 2,2’-(9,9-Dioctyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane]?2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-di-n-octylfluorene?2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-dioctylfluorene
• Storage: 2-8°C
• IUPAC Name: 2-[9,9-dioctyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluoren-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• InChI: InChI=1S/C41H64B2O4/c1-11-13-15-17-19-21-27-41(28-22-20-18-16-14-12-2)35-29-31(42-44-37(3,4)38(5,6)45-42)23-25-33(35)34-26-24-32(30-36(34)41)43-46-39(7,8)40(9,10)47-43/h23-26,29-30H,11-22,27-28H2,1-10H3
• InChIKey: FAHIZHKRQQNPLC-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)C4=C(C3(CCCCCCCC)CCCCCCCC)C=C(C=C4)B5OC(C(O5)(C)C)(C)C

9,9-Dioctylfluorene-2,7-diboronic acid bis(pinacol) ester (Cat No.:R015001) is a chemical compound. It is a derivative of fluorene containing two boronic acid functional groups substituted at positions 2 and 7, protected with pinacol ester groups. This compound is commonly used in organic synthesis as a versatile building block for the preparation of various functional materials, such as conjugated polymers, OLEDs (organic light-emitting diodes), and other electronic and optoelectronic devices. Its unique structure enables efficient coupling reactions with other molecules, making it valuable in the field of materials chemistry and electronics.