2,4,6-Trichlorophenylboronic acid

2,4,6-Trichlorophenylboronic acid (CAS: 73852-18-3) is a high-purity trichlorine-substituted aromatic boronic acid fine chemical intermediate. It features a stable benzene ring structure with three chlorine atom substitutions and active boronic acid functional groups, possessing excellent chemical stability, electron-withdrawing performance and organic reaction activity. This product has moderate solubility in polar organic solvents, low side reaction rate and stable batch consistency. 2,4,6-Trichlorophenylboronic acid (CAS: 73852-18-3) is widely used in Suzuki cross-coupling reactions, halogenated aromatic compound derivatization and pharmaceutical intermediate synthetic manufacturing.

2,4,6-Trichloro-benzeneboronic acid, 2,4,6-Trichlorobenzeneboronic acid, Boronic acid, 2,4,6-trichlorophenyl, 2,4,6-Trichloroarylboronic acid

1. Halogenated Aromatic Pharmaceutical Intermediate Synthesis Application: 2,4,6-Trichlorophenylboronic acid (CAS: 73852-18-3) serves as a core building block for synthesizing trichlorinated aromatic pharmaceutical intermediates. The special trichlorine-substituted structure optimizes the lipophilicity and biological activity of drug molecules, supporting the R&D and industrial production of antibacterial, antifungal and pesticide pharmaceutical intermediates. 2. Industrial Suzuki Cross-Coupling Reaction Application: 2,4,6-Trichlorophenylboronic acid (CAS: 73852-18-3) is a high-efficiency monomer for industrial halogenated aromatic cross-coupling processes. It maintains high reaction conversion efficiency under mild catalytic conditions, effectively reduces impurity generation in continuous production, and meets high-purity manufacturing standards of complex chlorinated fine chemicals. 3. Functional Chlorinated Fine Chemical Derivatization Application: 2,4,6-Trichlorophenylboronic acid (CAS: 73852-18-3) is applied to structural functional modification of halogenated fine chemicals. The active boronic acid group supports diversified substitution and cyclization reactions, realizing customized derivatization of high-value trichlorinated aromatic functional compounds. 4. Laboratory Organic Synthesis Research Application:2,4,6-Trichlorophenylboronic acid (CAS: 73852-18-3) acts as a standard experimental reagent for researching multi-chlorine substituted aromatic boronic acid reaction mechanisms, providing stable high-purity raw material support for new halogenated organic compound development and synthetic process optimization.

98%

C6H4BCl3O2

225.27

2 years under proper storage

White to Off-white Crystalline Powder

Research Grade, Synthetic Grade, Fine Chemical Grade

1.56±0.1 g/cm3