4- (Hydroxymethyl) phenylboronic acid

4- (Hydroxymethyl) phenylboronic acid (CAS: 59016-93-2) is a high-purity hydroxymethyl-functionalized aromatic boronic acid fine chemical. The molecular structure consists of a phenylboronic acid skeleton modified with a para-hydroxymethyl active group, featuring mild reaction activity, excellent hydrophilic and organic solvent solubility, and stable chemical properties under conventional synthetic conditions. This monosubstituted boronic acid has low hydrolysis rate and high coupling selectivity, supporting efficient and low-side-reaction organic synthesis. 4- (Hydroxymethyl) phenylboronic acid (59016-93-2) acts as a versatile bifunctional building block, extensively used in fine organic synthesis, pharmaceutical intermediate modification and functional molecular customization for industrial and laboratory applications.

4-Hydroxymethylphenylboronic acid, (4- (Hydroxymethyl) phenyl) boronic acid, p-Hydroxymethylphenylboronic acid, 4-Boronobenzyl alcohol

29319000

1. Versatile Suzuki Cross-Coupling Synthesis 4- (Hydroxymethyl) phenylboronic acid (CAS: 59016-93-2) is a universal monomer for high-efficiency Suzuki-Miyaura cross-coupling reactions. The retained hydroxymethyl functional group enables post-coupling structural derivation, which can be further etherified, esterified or oxidized to construct complex functional molecules, meeting industrial batch synthesis requirements of high-purity substituted aromatic fine chemicals. 2. Pharmaceutical Intermediate Derivatization 4- (Hydroxymethyl) phenylboronic acid (59016-93-2) is a critical precursor for the preparation of hydroxymethyl-substituted pharmaceutical intermediates. The active hydroxymethyl and boronic acid dual reactive sites optimize molecular binding activity, supporting the R&D and scale-up production of anti-tumor, antibacterial and anti-inflammatory targeted drug intermediates. 3. Functional Biochemical Probe Preparation 4- (Hydroxymethyl) phenylboronic acid (CAS: 59016-93-2) is widely applied in customized synthesis of biochemical detection probes and biological functional materials. Its balanced hydrophilicity and lipophilicity improve molecular solubility in mixed solvents, while dual reactive groups provide accurate modification sites for probe molecular assembly and functional optimization.

≥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 boronic acid hydrolysis and hydroxymethyl group oxidation

2 years under proper storage

White to off-white crystalline powder

Research Grade, Fine Chemical Grade

1.27±0.1 g/cm3