While 3-Aminophenylboronic Acid Monohydrate (CAS 206658-89-1) is widely recognized for its crucial role as a pharmaceutical intermediate, its versatility extends far beyond drug development. This bifunctional molecule, bearing both an amino group and a boronic acid moiety, is a powerful tool in the arsenal of organic chemists and materials scientists, enabling a wide range of advanced applications.

In organic synthesis, the boronic acid group of 3-Aminophenylboronic Acid Monohydrate is exceptionally adept at participating in palladium-catalyzed cross-coupling reactions, most notably the Suzuki-Miyaura coupling. This reaction is fundamental for creating carbon-carbon bonds, allowing for the construction of complex biaryl systems. These systems are not only prevalent in pharmaceuticals but also form the backbone of many advanced materials, including organic semiconductors used in OLEDs and conductive polymers for electronics. When researchers need to buy these specialized building blocks for materials science, a reliable manufacturer offering high-purity 3-Aminophenylboronic Acid Monohydrate is invaluable.

The amino group on the phenyl ring adds another layer of reactivity. It can serve as an anchoring point for further functionalization, polymerization, or immobilization onto surfaces. This makes 3-Aminophenylboronic Acid Monohydrate a key component in the development of smart materials and biosensors. For example, its ability to reversibly bind with diols has been exploited to create glucose-sensitive hydrogels and drug delivery systems that respond to physiological changes. Such innovations are critical for advancements in areas like diabetes management and targeted therapy.

Moreover, the compound finds application in the field of supramolecular chemistry. Its capacity to form directional hydrogen bonds and coordinate with other molecules allows for the self-assembly of intricate structures, such as macrocyclic compounds and molecular cages. These sophisticated assemblies have potential applications in molecular recognition, catalysis, and separation technologies. Sourcing these unique intermediates often involves connecting with specialized suppliers who understand the nuances of advanced chemical synthesis and can provide the necessary materials with consistent quality.

For R&D departments looking to innovate, the ability to easily access and purchase compounds like 3-Aminophenylboronic Acid Monohydrate is essential. Competitive pricing from direct manufacturers, especially those based in regions like China, can make ambitious research projects more feasible. It is always advisable to inquire about product specifications, stability, and optimal storage conditions. For instance, as a monohydrate, its handling and storage require attention to maintain its integrity for synthesis. A thorough understanding of its properties and a robust procurement strategy, perhaps involving obtaining a quote for bulk quantities or custom synthesis, will ensure that its full potential in advanced chemical applications is realized.

In summary, 3-Aminophenylboronic Acid Monohydrate is far more than just a pharmaceutical intermediate. Its dual functionality and reactive nature make it a cornerstone for innovation in organic synthesis, materials science, and beyond. Partnering with reputable suppliers who can guarantee quality and availability is key to unlocking its full potential in these diverse and exciting fields.