2-Vinylphenylboronic acid

2-Vinylphenylboronic acid (CAS: 15016-42-9) is a high-purity functional boronic acid fine chemical and dual-functional organic synthetic intermediate. It possesses a special molecular structure containing both vinyl active group and boronic acid functional group on the ortho-position of benzene ring, featuring moderate chemical activity, excellent reaction selectivity and good solubility in conventional organic solvents. The dual reactive sites enable the compound to undergo both vinyl polymerization and boronic acid coupling reactions, with stable chemical properties under low-temperature and sealed storage conditions. 2-Vinylphenylboronic acid (15016-42-9) is widely used in Suzuki coupling synthesis, functional polymer material modification and fine chemical derivatization in industrial and laboratory fields.

(2-Ethenylphenyl) boronic acid, 2-Boronostyrene, o-Vinylphenylboronic acid, 2-Ethenylbenzeneboronic acid

2931900090

1. Suzuki Cross-Coupling Reaction Synthesis 2-Vinylphenylboronic acid (CAS: 15016-42-9) serves as a high-efficiency aromatic boronic acid coupling reagent. The active boronic acid group can efficiently participate in Suzuki cross-coupling reactions with halogenated aromatic compounds, stably constructing vinyl-substituted biphenyl and heterocyclic molecular skeletons, supporting high-purity fine organic synthesis and industrial scale-up production. 2. Functional Polymer Material Modification 2-Vinylphenylboronic acid (15016-42-9) is a key monomer for functional polymer preparation. The reactive vinyl group can undergo free radical polymerization and copolymerization reactions, introducing boronic acid functional groups into polymer molecular chains to prepare boron-containing functional polymers with specific recognition and adsorption properties, which are widely applied in new material research and industrial production. 3. Fine Chemical Derivatization Processing 2-Vinylphenylboronic acid (CAS: 15016-42-9) is used for structural derivatization of high-end fine chemicals. It can undergo esterification, substitution and grafting reactions through boronic acid active sites to synthesize various vinyl aromatic boronic acid derivatives, which are commonly used in chemical additives and organic functional material intermediates. 4. Biomedical Intermediate Preparation 2-Vinylphenylboronic acid (15016-42-9) is applied in the synthesis of biomedical intermediates. Its unique dual-functional structure can optimize the molecular recognition performance and biological activity of target compounds, providing reliable raw material support for the research and development of biosensor monomers and targeted biomedical materials.

≥98%

Store at 2-8 °C in dry, sealed, dark and well-ventilated environment, avoid high temperature, humid air and long-term light exposure to prevent polymerization and hydrolysis deterioration

2 years under proper storage

White to off-white crystalline powder

Research Grade, Fine Chemical Grade, Organic Synthetic Intermediate Grade, Coupling Reaction Grade

1.1±0.1 g/cm3

105-107 °C