3-(Aminomethyl)benzeneboronic acid hydrochloride
95%
blur_circular Chemical Specifications
description Product Description
This bifunctional compound, featuring a boronic acid group and an aminomethyl substituent on a benzene ring, is widely utilized in organic synthesis. The boronic acid moiety is particularly valuable in Suzuki-Miyaura cross-coupling reactions, acting as a key building block for creating complex biaryl structures and facilitating carbon-carbon bond formation, which is essential in the production of pharmaceuticals, agrochemicals, and advanced materials. The aminomethyl group provides an additional reactive site for further derivatization, such as forming amide or amine linkages, enhancing its role as a crucial intermediate in the development of enzyme inhibitors, receptor ligands, and bioactive molecules for drug discovery and biochemical research. Its stability, reactivity, and versatility also make it valuable in the design of sensors and probes for detecting specific biomolecules in diagnostic applications.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | white solid |
| Purity | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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