3-Formylbenzeneboronic acid

3-Formylbenzeneboronic acid (CAS 87199-16-4) is a high-purity aldehyde-functionalized aromatic boronic acid fine chemical. Featured with air and moisture sensitivity, stable organic solubility and excellent Suzuki cross-coupling reactivity, this compound contains active aldehyde and boronic acid bifunctional groups on the benzene ring, providing flexible molecular modification capabilities.3-Formylbenzeneboronic acid (CAS 87199-16-4) serves as a core multifunctional synthetic building block, widely applied in pharmaceutical intermediate synthesis, organic functional molecule derivation and industrial fine chemical production.

29319090

1. Suzuki Cross-Coupling Reaction Synthesis: 3-Formylbenzeneboronic acid (CAS 87199-16-4) is a key bifunctional monomer for high-efficiency Suzuki-Miyaura cross-coupling reactions. It can stably react with various halogenated aromatic compounds to construct aldehyde-substituted biaryl skeletons, supporting batch production of high-purity functional aromatic intermediates for industrial organic synthesis. 2. Pharmaceutical Intermediate Derivatization: 3-Formylbenzeneboronic acid (CAS 87199-16-4) is an essential modular intermediate for new drug development. It is widely used in the synthesis of antiviral, anti-inflammatory and targeted therapeutic drug intermediates, and serves as a critical raw material for the preparation of protease inhibitor drugs. 3. Functional Organic Material Modification: 3-Formylbenzeneboronic acid (CAS 87199-16-4) possesses dual active reaction sites of aldehyde and boronic acid. It supports multi-step functional group transformation and structural grafting reactions, meeting customized production demands of high-value organic fine chemical derivatives and polymer functional materials. 4. Laboratory Organic Synthetic Research: 3-Formylbenzeneboronic acid (CAS 87199-16-4) 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 process optimization of aldehyde-containing aromatic compounds in chemical and pharmaceutical research institutions.

≥98%

C7H7BO3

149.94

2 years under proper storage

Off-white to beige crystalline powder

Laboratory Grade, Industrial Grade

1.24±0.1 g/cm3

182-186°C