Description

Benzenamine, 2,4,6-Trimethyl-N,n-Bis[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]- is a sophisticated, multi-functional aromatic amine derivative featuring two pinacol boronate ester groups. This compound is a critical advanced intermediate in modern synthetic chemistry, prized for its dual functionality which enables precise molecular construction. It is primarily sought after by research chemists and process development scientists in the pharmaceutical, agrochemical, and materials science sectors for constructing complex organic architectures.

Application

• Suzuki-Miyaura Cross-Coupling Reactions: Serves as a key boron-containing coupling partner for the synthesis of biaryl and heterobiaryl structures, a cornerstone reaction in drug discovery.
• Pharmaceutical Intermediate: Used in the research and development of active pharmaceutical ingredients (APIs), particularly for candidates targeting central nervous system and oncology pathways.
• Agrochemical Synthesis: Employed in creating novel herbicides, fungicides, and insecticides with enhanced efficacy and selectivity.
• Organic Electronic Materials: Acts as a building block for conjugated polymers and small molecules used in OLEDs, OFETs, and perovskite solar cells.
• Ligand and Catalyst Development: Utilized to synthesize novel nitrogen-containing ligands for transition metal catalysis.
• Chemical Biology Probes: Facilitates the creation of tagged molecules for studying biological processes and target engagement.

Basic Information

Item	Detail
Product Name	Benzenamine, 2,4,6-Trimethyl-N,n-Bis[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]-
CAS No.	1282616-14-1
Molecular Formula	C34H45B2NO4
Molecular Weight	553.35 g/mol
Synonyms	N,N-Bis[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,4,6-trimethylbenzenamine; 2,4,6-Trimethyl-N,N-bis[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]aniline; Tris(4-boronic acid pinacol ester phenyl)amine derivative; Boronate ester functionalized triarylamine; Advanced Suzuki coupling reagent; Aromatic amine boronic ester
EINECS	Contact for details

Quality Control

Every batch of our Benzenamine, 2,4,6-Trimethyl-N,n-Bis[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]- is synthesized and purified under controlled conditions to ensure high chemical purity and lot-to-lot consistency, meeting the stringent requirements of research and process chemistry. Our products undergo rigorous quality testing to ensure compliance with industry standards. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at 2-8°C under an inert atmosphere (e.g., nitrogen or argon) due to its moisture-sensitive and easily oxidized nature. Allow the container to reach room temperature before opening to prevent moisture condensation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	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.