5-Borono-2-chlorobenzoic acid

5-Borono-2-chlorobenzoic acid (CAS 913835-32-2) is a high-purity halogen-substituted aromatic boronic acid fine chemical. The molecular structure integrates chloro substituent, carboxyl group and boronic acid functional group on the benzene ring, featuring stable chemical properties, moderate water solubility and efficient Suzuki cross-coupling reaction activity. The dual active functional groups enable diversified molecular derivatization, while the halogen substitution structure optimizes molecular stability and reaction selectivity. 5-Borono-2-chlorobenzoic acid (CAS 913835-32-2) serves as a core bifunctional aromatic building block, widely applied in pharmaceutical intermediate synthesis, heterocyclic compound derivation and high-end fine chemical customized production.

2931909090

1. Suzuki Cross-Coupling Synthesis: 5-Borono-2-chlorobenzoic acid (CAS 913835-32-2) is a high-selectivity halogenated boronic acid coupling reagent. Its unique chloro-carboxyl bifunctional structure supports precise aromatic skeleton construction, enabling efficient synthesis of multi-substituted benzoic acid derivatives for fine chemical industrial production. 2. Pharmaceutical Intermediate Derivatization: 5-Borono-2-chlorobenzoic acid (CAS 913835-32-2) is an important modular intermediate for innovative drug R&D. The halogen and carboxyl active groups can effectively optimize molecular biological activity, widely used in the synthesis of anti-inflammatory, antibacterial and heterocyclic therapeutic drug intermediates. 3. Heterocyclic Compound Preparation: 5-Borono-2-chlorobenzoic acid (CAS 913835-32-2) can undergo cyclization and cross-coupling reactions to construct complex nitrogen-containing and oxygen-containing heterocyclic compounds, meeting the customized synthesis demands of high-value heterocyclic fine chemicals. 4. Laboratory Organic Chemistry Research: 5-Borono-2-chlorobenzoic acid (CAS 913835-32-2) is a standard high-purity laboratory reagent. With stable batch consistency and controllable bifunctional reaction characteristics, it is suitable for organic reaction mechanism verification and new compound structural modification research.

≥98%

C7H6BClO4

200.39

2 years under proper storage

White to light yellow crystalline powder

Laboratory Grade, Industrial Grade

1.57±0.1 g/cm3

154-156°C