4-Acetylphenylboronic acid

4-Acetylphenylboronic acid (CAS: 149104-90-5) is a high-purity carbonyl-functionalized aromatic boronic acid fine chemical. Its molecular structure integrates para-acetyl active groups and boronic acid reactive sites, featuring dual functional reactivity, stable chemical properties and high synthesis selectivity. This functional organic boron compound is soluble in conventional anhydrous organic solvents and slightly soluble in water, with excellent molecular derivatization performance. 4-Acetylphenylboronic acid (149104-90-5) acts as a critical bifunctional synthetic building block, widely used in carbonyl-containing aromatic derivative preparation, pharmaceutical intermediate synthesis and high-end fine chemical industrial customization.

4-Formylphenylboronic acid, 4-Acetylbenzeneboronic acid, (4-Acetylphenyl) boronic acid, p-Acetylphenylboronic acid

29319000

1. Functionalized Suzuki Coupling Synthesis Monomer 4-Acetylphenylboronic acid (CAS: 149104-90-5) is a core bifunctional monomer for high-precision Suzuki-Miyaura cross-coupling reactions. The retained acetyl active group enables secondary structural modification after coupling synthesis, effectively expanding molecular design diversity. It is widely used in industrial batch synthesis of carbonyl-substituted aromatic fine chemicals and complex molecular intermediates. 2. Pharmaceutical Intermediate Derivatization Production 4-Acetylphenylboronic acid (149104-90-5) serves as an essential precursor for the synthesis of carbonyl-containing pharmaceutical intermediates. The acetyl and boronic acid dual active structures support multi-step derivation reactions, which can be used to prepare anti-tumor, anti-inflammatory and antibacterial small-molecule drug intermediates, meeting the raw material requirements for pharmaceutical laboratory R&D and industrial scale-up production. 3. Custom Fine Chemical Molecular Modification 4-Acetylphenylboronic acid (CAS: 149104-90-5) is commonly applied in customized multi-step organic synthesis and functional molecular modification. Its stable aromatic skeleton and dual reactive sites provide accurate reaction positions for molecular assembly, supporting the customized production of high-end functional fine chemicals and biochemical molecular probes.

≥98%

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Store at 2-8 °C in dry, sealed, dark and inert nitrogen environment, away from moisture, high temperature and strong oxidants to prevent hydrolysis and structural decomposition

2 years under proper storage

White to off-white crystalline powder

Research Grade, Fine Chemical Grade

1.21±0.1 g/cm3