3-Borono-2-methoxybenzoic acid

3-Borono-2-methoxybenzoic acid (CAS 913836-10-9) is a high-purity difunctional substituted aromatic boronic acid fine chemical. The molecular structure contains ortho-methoxy, meta-boronic acid and carboxylic acid functional groups on the benzene ring, featuring stable chemical properties, moderate organic solubility and excellent Suzuki cross-coupling reactivity. The triple functional group structure enables diversified molecular derivatization and structural modification, making it a versatile synthetic building block. 3-Borono-2-methoxybenzoic acid (CAS 913836-10-9) is widely utilized in pharmaceutical intermediate synthesis, biaryl compound preparation and customized fine chemical synthesis.

2931909090

1. Suzuki Cross-Coupling Synthesis: 3-Borono-2-methoxybenzoic acid (CAS 913836-10-9) serves as a high-efficiency difunctional boronic acid coupling reagent. It can undergo high-selectivity cross-coupling reactions with halogenated aromatic compounds to synthesize high-purity methoxy and carboxyl substituted biaryl derivatives, supporting industrial batch production of complex fine chemical intermediates. 2. Pharmaceutical Intermediate Derivatization: 3-Borono-2-methoxybenzoic acid (CAS 913836-10-9) is a core modular intermediate for new drug research and development. The unique trisubstituted benzene skeleton can effectively optimize the molecular solubility, stability and biological activity of drug compounds, and is commonly used in the synthesis of anti-inflammatory, analgesic and targeted therapeutic drug intermediates. 3. Functional Fine Chemical Customized Synthesis: 3-Borono-2-methoxybenzoic acid (CAS 913836-10-9) has multiple active functional groups with adjustable reaction characteristics. It supports multi-step molecular structural modification and derivatization, meeting the customized production demands of high-value substituted aromatic fine chemicals and downstream derivative products. 4. Laboratory Organic Synthetic Research: 3-Borono-2-methoxybenzoic acid (CAS 913836-10-9) is a standard high-purity laboratory reagent. With stable batch consistency and controllable dual-group reaction performance, it is widely applied in organic reaction mechanism verification and synthesis research of multi-functional substituted benzoic acid derivatives.

≥98%

C8H9BO5

195.97

2 years under proper storage

White to off-white crystalline powder

Laboratory Grade, Industrial Grade

1.39±0.1 g/cm3

152-155°C