Description

2,4-Diphenyl-6-[3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]-1,3,5-Triazine is a high-value, functionalized triazine derivative containing a key pinacol boronate ester group. This compound matters as a versatile and crucial building block in modern synthetic chemistry, enabling the formation of new carbon-carbon bonds via cross-coupling reactions. It is primarily needed by researchers and manufacturers in the pharmaceutical, agrochemical, and materials science sectors for developing advanced organic electronic materials, active pharmaceutical ingredients (APIs), and novel chemical entities.

Application

• Suzuki-Miyaura Cross-Coupling Reactions: Acts as a critical boron-containing coupling partner for synthesizing complex biaryl and heterobiaryl structures prevalent in drug discovery.
• Pharmaceutical Intermediate: Serves as a key precursor in the synthesis of potential active pharmaceutical ingredients (APIs), especially those containing triazine cores for therapeutic applications.
• Organic Light-Emitting Diodes (OLEDs): Used as an electron-transport material or host material in the fabrication of high-performance OLED devices for displays and lighting.
• Agrochemical Synthesis: Employed in the research and development of novel herbicides, fungicides, and insecticides that utilize triazine chemistry.
• Ligand and Catalyst Development: Functionalized to create novel ligands for transition metal catalysts used in asymmetric synthesis and other catalytic processes.
• Polymer and Materials Science: Incorporated into polymers to modify electronic properties, creating materials for organic photovoltaics (OPVs) and other advanced electronic applications.
• Chemical Research & Development: A valuable reagent for academic and industrial R&D labs exploring new synthetic methodologies and novel molecular architectures.

Basic Information

Product Name	2,4-Diphenyl-6-[3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]-1,3,5-Triazine
CAS No.	1269508-31-7
Molecular Formula	C31H28BN3O2
Molecular Weight	485.39 g/mol
Synonyms	[3-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl]boronic acid pinacol ester; 2-[3-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; 3-(4,6-Diphenyl-1,3,5-triazin-2-yl)benzeneboronic acid pinacol ester; 2,4-Diphenyl-6-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine; Triazine boronic ester; B-Triazine pinacol boronate
EINECS	Contact for details

Quality Control

Our production of this advanced intermediate adheres to strict quality control protocols to ensure batch-to-batch consistency and high purity, which is critical for sensitive cross-coupling reactions. Each lot is characterized using advanced analytical techniques including NMR (1H, 13C, 11B), HPLC, and mass spectrometry. Comprehensive Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment to support your R&D and scale-up activities.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at a controlled room temperature (15-25°C) in a cool, dry, and well-ventilated place. Due to its hygroscopic and easily oxidized nature, the container must be kept tightly sealed when not in use to minimize exposure to moisture and air.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.