(3-Acrylamidophenyl) boronic acid

(3-Acrylamidophenyl) boronic acid (CAS 99349-68-5) is a high-purity acrylamide-functionalized aromatic boronic acid fine chemical, which contains trace anhydride impurities in commercial industrial batches. The compound integrates reactive acrylamide vinyl groups and boronic acid functional groups, possessing dual polymerization and cross-coupling reaction activity. It features stable chemical properties under low-temperature sealed storage and good solubility in conventional organic solvents. (3-Acrylamidophenyl) boronic acid (CAS 99349-68-5) serves as a core dual-functional synthetic building block, widely applied in functional polymer modification, biocompatible material preparation and pharmaceutical intermediate synthesis.

2931909090

1. Suzuki Cross-Coupling Organic Synthesis: (3-Acrylamidophenyl) boronic acid (CAS 99349-68-5) is a high-activity monomer for Suzuki-Miyaura cross-coupling reactions. Its stable acrylamide-substituted benzene structure can efficiently couple with halogenated compounds to construct functionalized biaryl skeletons, supporting industrial synthesis of high-value fine chemical intermediates with polymerization activity. 2. Functional Polymer Material Modification: (3-Acrylamidophenyl) boronic acid (CAS 99349-68-5) is widely used for the modification and copolymerization of acrylic polymer materials. The dual reactive functional groups enable molecular grafting and cross-linking, effectively improving the structural stability and functional diversity of polymer materials. 3. Biocompatible Material Preparation: (3-Acrylamidophenyl) boronic acid (CAS 99349-68-5) is a key raw material for preparing boronic acid-based responsive hydrogels and biocompatible materials. It can realize specific molecular recognition and reversible bonding, which is applied in biosensing and drug carrier material research and production. 4. Pharmaceutical Intermediate Derivatization: (3-Acrylamidophenyl) boronic acid (CAS 99349-68-5) is an important modular intermediate for new drug development. The unique dual-functional structure provides abundant molecular modification sites, supporting the synthesis of targeted therapeutic drug intermediates with high biological activity.

98%

C9H10BNO3

190.99

2 years under proper storage

White to off-white crystalline solid

Laboratory Grade, Industrial Grade