Description

2,4-Diphenyl-6-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine (CAS No. 1696425-27-0) is a high-purity boronate ester-functionalized triazine derivative with the molecular formula C₂₇H₂₆BN₃O₂. This compound features a 1,3,5-triazine core substituted with two phenyl groups and a 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl moiety, making it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions and other boron-mediated transformations. The presence of the pinacol boronate ester group enhances its stability and reactivity under mild conditions. Ideal for pharmaceutical research, materials science, and organic synthesis, this compound is supplied as a crystalline solid with ≥95% purity (HPLC). Store under inert conditions at 2-8°C to maintain stability.

Properties

• CAS Number: 1696425-27-0
• Complexity: 605
• IUPAC Name: 2,4-diphenyl-6-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine
• InChI: InChI=1S/C27H26BN3O2/c1-26(2)27(3,4)33-28(32-26)22-18-12-11-17-21(22)25-30-23(19-13-7-5-8-14-19)29-24(31-25)20-15-9-6-10-16-20/h5-18H,1-4H3
• InChI Key: LILSOUBYWPFKOI-UHFFFAOYSA-N
• Exact Mass: 435.2118072
• Molecular Formula: C27H26BN3O2
• Molecular Weight: 435.3
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2C3=NC(=NC(=N3)C4=CC=CC=C4)C5=CC=CC=C5
• Topological: 57.1
• Monoisotopic Mass: 435.2118072
• Synonyms: 2,4-Diphenyl-6-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine, 1696425-27-0, 1,3,5-Triazine, 2,4-diphenyl-6-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl], SCHEMBL17529962, MFCD32670110, SY300362, G71163, 2-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenylboronic Acid Pinacol Ester

Application

This compound is widely used as a key building block in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl and heteroaryl structures in drug discovery and materials science. Its boronate ester group enables efficient Pd-catalyzed coupling with aryl halides, making it valuable for constructing complex organic frameworks. Researchers also utilize it in the development of luminescent materials and supramolecular chemistry due to its rigid triazine core and aromatic substituents.

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