(4-Hydroxy-3-methylphenyl) boronic acid

(4-Hydroxy-3-methylphenyl) boronic acid (CAS 762263-66-1) is a high-purity hydroxyl-methyl dual-functional substituted aromatic boronic acid fine chemical. This compound features high chemical stability, strong moisture sensitivity and excellent organic solubility, retaining efficient Suzuki cross-coupling reactivity. With active phenolic hydroxyl and boronic acid functional groups on the benzene ring, it possesses superior molecular modification and derivatization capabilities. (4-Hydroxy-3-methylphenyl) boronic acid (CAS 762263-66-1) serves as a core bifunctional synthetic building block, widely applied in pharmaceutical intermediate synthesis, fine chemical derivatization and laboratory organic synthesis research.

2931900090

1. Suzuki Cross-Coupling Organic Synthesis: (4-Hydroxy-3-methylphenyl) boronic acid (CAS 762263-66-1) is a key monomer for high-efficiency Suzuki-Miyaura cross-coupling reactions. It can stably react with various halogenated aromatic compounds to construct hydroxyl-methyl substituted biaryl skeletons, supporting batch production of high-purity functional aromatic intermediates for industrial organic synthesis. 2. Pharmaceutical Intermediate Derivatization: (4-Hydroxy-3-methylphenyl) boronic acid (CAS 762263-66-1) is an essential modular intermediate for new drug development. The dual active functional groups enable diversified structural modification, widely used in the synthesis of anti-inflammatory, antibacterial and targeted therapeutic drug intermediates in the pharmaceutical industry. 3. Functional Fine Chemical Customization: (4-Hydroxy-3-methylphenyl) boronic acid (CAS 762263-66-1) contains multiple active reaction sites. It supports multi-step functional group transformation and structural grafting reactions, meeting customized production demands of high-value hydroxyl-substituted aromatic fine chemical derivatives. 4. Laboratory Synthetic Research & Optimization: (4-Hydroxy-3-methylphenyl) boronic acid (CAS 762263-66-1) is a standard high-purity laboratory research reagent. With stable batch consistency and controllable reaction activity, it is commonly used for organic reaction mechanism verification and synthesis process optimization of bifunctional substituted aromatic compounds in scientific research institutions.

98%

C7H9BO3

151.96

2 years under proper storage

White to off-white crystalline powder

Laboratory Grade, Industrial Grade

1.26±0.1 g/cm3

212-216°C