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CAS 912844-88-3

2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI B6023

2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI B6023

Chemical Identity

Other names
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)biphenyl · 3-Biphenylboronic Acid Pinacol Ester
CAS No.
912844-88-3
PubChem
CID 17942655·SID 468590855
Formula
C18H21BO2
Molecular weight
280.17 g/mol
Purity
>98.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4,4,5,5-tetramethyl-2-(3-phenylphenyl)-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC=C2)C3=CC=CC=C3
InChIKey
UUMDSELMDKINPL-UHFFFAOYSA-N
MDL
MDL18452169
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TCI B6023 2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron reagent in the form of a pinacol ester of 3-biphenylboronic acid, primarily utilized in Suzuki-Miyaura cross-coupling reactions for constructing carbon-carbon bonds. This compound introduces the biphenyl moiety into target molecules with high efficiency, making it a valuable building block in organic synthesis. It is widely applied in pharmaceutical development, functional organic material research, and medicinal chemistry laboratories requiring biphenyl-containing molecular architectures.

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