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CAS 850264-92-5

3,3'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl TCI B5704

3,3'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl TCI B5704

Chemical Identity

Other names
3,3'-Biphenyldiboronic Acid Bis(pinacol) Ester
CAS No.
850264-92-5
PubChem
CID 66806859·SID 468590662
Formula
C24H32B2O4
Molecular weight
406.14 g/mol
Purity
>98.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4,4,5,5-tetramethyl-2-[3-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]phenyl]-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC=C2)C3=CC=CC(=C3)B4OC(C(O4)(C)C)(C)C
InChIKey
CDDAYWROTQQONU-UHFFFAOYSA-N
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TCI B5704 (CAS 850264-92-5), 3,3'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl, is a bifunctional organoboron reagent designed for Suzuki-Miyaura cross-coupling reactions, particularly in the construction of biphenyl-based conjugated polymers and porous organic frameworks. Its dual pinacol boronate ester groups at the meta positions enable stepwise or simultaneous carbon-carbon bond formation with aryl halides under palladium catalysis. This compound finds broad utility in the synthesis of COFs, MOFs, optoelectronic materials, and advanced functional polymers for research and development applications.

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