4-Acetylaminophenylboronic acid

4-Acetylaminophenylboronic acid (CAS: 101251-09-6) is a high-purity amide-functionalized aromatic boronic acid fine chemical. The molecular structure consists of para-acetylamino substituted benzene ring and active boronic acid functional groups, featuring dual reactive characteristics of amide group and boronic acid group, excellent chemical stability and selective reaction activity. This functional organic boron compound is soluble in polar anhydrous organic solvents and slightly soluble in water, with outstanding molecular derivatization and coupling performance. 4-Acetylaminophenylboronic acid (101251-09-6) is a key bifunctional synthetic building block, widely used in amide-containing aromatic derivative preparation, biomedical intermediate synthesis and high-end fine chemical industrial customization.

4-Acetamidophenylboronic acid, p-Acetamidophenylboronic acid, 4-Acetamidobenzeneboronic acid, (4-Acetylaminophenyl) boronic acid

29319000

1. Amide Functionalized Suzuki Coupling Monomer 4-Acetylaminophenylboronic acid (CAS: 101251-09-6) serves as a core high-selectivity monomer for Suzuki-Miyaura cross-coupling reactions. The stable acetylamino functional group avoids side reactions during coupling synthesis and can be retained for subsequent structural modification, greatly enriching the diversity of aromatic molecular design. It is widely used in industrial batch synthesis of high-purity amide-substituted aromatic fine chemicals. 2. Biomedical and Pharmaceutical Intermediate Synthesis 4-Acetylaminophenylboronic acid (101251-09-6) is an important precursor for the preparation of biomedical small-molecule intermediates. The acetylamino aromatic structure has good biocompatibility and molecular modifiability, which can be used to synthesize anti-inflammatory, analgesic and targeted therapeutic drug intermediates, supporting pharmaceutical laboratory research and industrial scale-up production. 3. Custom Functional Fine Chemical Modification 4-Acetylaminophenylboronic acid (CAS: 101251-09-6) is widely applied in customized multi-step organic synthesis and functional molecular modification. Its dual active sites of amide and boronic acid provide accurate reaction positions for molecular assembly, meeting the high-precision raw material requirements for customized production of biochemical probes and high-end functional fine chemicals.

≥97%

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

2 years under proper storage

White to off-white crystalline powder

Research Grade, Fine Chemical Grade, Pharmaceutical Intermediate Grade

1.28±0.1 g/cm3