4-Iodophenylboronic acid

4-Iodophenylboronic acid (CAS 5122-99-6) is a high-purity iodine-substituted aromatic boronic acid fine chemical. It features a stable benzene ring structure grafted with iodine functional groups and active boronic acid reactive sites, possessing excellent organic solubility, unique photochemical properties and efficient Suzuki cross-coupling reactivity. This product is light and moisture sensitive, prone to photodegradation and hydrolysis under harsh conditions, requiring low-temperature sealed inert gas storage to stabilize chemical activity and product purity. 4-Iodophenylboronic acid (CAS 5122-99-6) is a critical halogenated aromatic synthetic building block, widely applied in pharmaceutical intermediate derivation, organic material synthesis and fine chemical customized production.

29319090

1. Suzuki Cross-Coupling Reaction Synthesis: 4-Iodophenylboronic acid (CAS 5122-99-6) is a high-activity monomer for Suzuki cross-coupling reactions. Its para-iodine substituted benzene ring structure provides excellent reaction activity and selectivity, efficiently constructing complex functional aromatic molecular skeletons for high-precision fine chemical synthesis and industrial organic manufacturing. 2. Pharmaceutical Intermediate Manufacturing: 4-Iodophenylboronic acid (CAS 5122-99-6) serves as a core modular intermediate for new drug research and development. The unique iodo-functionalized structure optimizes molecular biological activity and target binding performance, supporting structural modification and derivation of anti-tumor and targeted therapeutic drug intermediates. 3. Functional Organic Material Preparation: 4-Iodophenylboronic acid (CAS 5122-99-6) acts as a key precursor for photoresponsive organic materials. Its special iodine substitution characteristics endow the compound with unique photochemical activity, applicable to the preparation of organic fluorescent probes, photoelectric materials and polymer functional monomers. 4. Laboratory Customized Organic Synthesis: 4-Iodophenylboronic acid (CAS 5122-99-6) is a standard high-purity laboratory reagent. With stable batch consistency and controllable reaction performance, it meets experimental demands of halogenated organic reaction mechanism verification and customized synthesis of new functional aromatic compounds.

98%

C6H6BIO2

247.83

2 years under proper storage

White to off-white crystalline powder

Laboratory Grade, Industrial Grade

1.95±0.1 g/cm3

326-330°C