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2,6-Dichlorophenylboronic acid

CAT: 1139-73852-17-2Size: 1 EachDry Ice: NoHazardous: No
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CAT#:1139-73852-17-2Size:1 Each
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Description
2,6-Dichlorophenylboronic acid (CAS 73852-17-2) is a high-purity dichloro-substituted aromatic boronic acid fine chemical. This compound features a benzene ring skeleton with dichloro ortho-disubstituted structure and active boronic acid functional groups, presenting typical moisture-sensitive chemical properties and stable performance under low-temperature sealed and dry storage conditions. It has excellent reaction activity for Suzuki-Miyaura cross-coupling and various organic derivatization reactions, with unique steric hindrance and electronic effects brought by double chlorine substitution. 2,6-Dichlorophenylboronic acid (CAS 73852-17-2) serves as a core dichlorinated aromatic building block, widely applied in pharmaceutical intermediate customization, agrochemical synthesis and high-end fine chemical derivatization.
Applications
1. Dichlorinated Aromatic Cross-Coupling Synthesis: 2,6-Dichlorophenylboronic acid (CAS 73852-17-2) is a key monomer for palladium-catalyzed Suzuki cross-coupling reactions. Its unique 2,6-dichloro substituted benzene structure optimizes reaction selectivity and stability, effectively reducing by-product generation, and is widely used for industrial synthesis of high-purity dichlorinated biaryl fine chemical intermediates. 2. Pharmaceutical Intermediate Customized Manufacturing: 2,6-Dichlorophenylboronic acid (CAS 73852-17-2) is an essential modular intermediate for new drug research and development. The ortho-dichloro structure can effectively adjust drug molecular lipophilicity and metabolic stability, supporting structural modification and customized synthesis of anti-inflammatory, antibacterial and targeted therapeutic small-molecule drug intermediates. 3. Agrochemical Fine Chemical Synthesis: 2,6-Dichlorophenylboronic acid (CAS 73852-17-2) acts as a critical precursor for high-efficiency pesticide and agrochemical intermediates. Its stable dichlorinated aromatic skeleton and active boronic acid groups support multi-step substitution and condensation reactions, enabling the preparation of high-activity agrochemical derivatives for modern agricultural chemical production. 4. Laboratory Organic Synthesis Research: 2,6-Dichlorophenylboronic acid (CAS 73852-17-2) is a standard high-purity laboratory synthetic reagent. With stable batch quality and unique ortho-dichloro aromatic reaction characteristics, it is widely used for organic reaction mechanism verification, synthetic route optimization and new functional compound development in scientific research projects.
Purity
99%
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.82
Shelf Life
2 years under proper storage
Appearance
Off-white crystalline powder
Grade
Laboratory Grade, Industrial Grade, Pharmaceutical Grade
Density
1.47±0.1 g/cm3
Melting Point
153°C
Boiling Point
341.8±52.0°C at 760 mmHg
EINECS
672-294-4