Description

n-Phenyl-n-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)-[1,1'-Biphenyl]-4-Amine is a high-value, advanced organic intermediate featuring a pinacol boronate ester functional group. This compound matters as a critical building block in modern cross-coupling reactions, enabling the precise construction of complex organic frameworks essential for advanced materials. It is primarily needed by R&D chemists and process engineers in the pharmaceutical, agrochemical, and organic electronics industries for synthesizing novel active ingredients and functional materials.

Application

• Pharmaceutical Intermediate: A key precursor in Suzuki-Miyaura cross-coupling reactions for the synthesis of novel drug candidates, particularly in oncology and CNS therapeutic areas.
• Agrochemical Synthesis: Used to create complex, bioactive molecules for next-generation herbicides, fungicides, and insecticides with improved efficacy.
• Organic Light-Emitting Diode (OLED) Materials: Serves as a building block for electron-transport layers (ETLs) and host materials in display and lighting technologies.
• Organic Photovoltaic (OPV) Research: Employed in the development of donor or acceptor materials for more efficient solar cells.
• Polymer Chemistry: Facilitates the synthesis of specialty polymers and dendrimers with tailored electronic or mechanical properties.
• Ligand and Catalyst Development: Used to construct sophisticated ligands for transition metal catalysts in asymmetric synthesis.
• Material Science Research: A versatile reagent for creating novel organic semiconductors and conductive polymers.
• Academic & Industrial R&D: A standard reagent for methodological development in synthetic organic chemistry laboratories worldwide.

Basic Information

Product Name	n-Phenyl-n-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)-[1,1'-Biphenyl]-4-Amine
CAS No.	1338803-75-0
Molecular Formula	C30H30BNO2
Molecular Weight	447.38 g/mol
Synonyms	4-(N-Phenyl-[1,1'-biphenyl]-4-ylamino)phenylboronic acid pinacol ester; N-Phenyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-[1,1'-biphenyl]-4-amine; N-Phenyl-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-biphenyl]-4-amine; TPBPA-Bpin; N-Phenyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)biphenyl-4-amine; [1,1'-Biphenyl]-4-amine, N-phenyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-; 4-(N-Phenylbiphenyl-4-ylamino)phenylboronic acid pinacol ester; N-Phenyl-4'-(pinacolatoboryl)-[1,1'-biphenyl]-4-amine
EINECS	Contact for details

Quality Control

Our n-Phenyl-n-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)-[1,1'-Biphenyl]-4-Amine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Products undergo rigorous analytical testing, including HPLC, NMR, and elemental analysis, to meet exacting customer specifications. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with each shipment to support your quality assurance and regulatory compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed under an inert atmosphere (e.g., nitrogen or argon) after opening to prevent degradation. Keep away from heat and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0% (Area %)
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals (as Pb)	≤ 20 ppm

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