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Structure of 65658-13-1
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(1H-Benzo[d]imidazol-4-yl)methanol features a benzimidazole core with a strategically positioned hydroxymethyl group, enabling facile functionalization in medicinal chemistry. This bench-stable scaffold integrates readily into bioactive molecules, offering enhanced solubility and hydrogen-bonding capacity for targeted ligand design.
(1H-Benzo[d]imidazol-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to biologically relevant heterocyclic scaffolds. Its benzimidazole core provides structural rigidity and hydrogen-bonding capacity, while the pendant alcohol facilitates derivatization via oxidation, esterification, or ether formation. The compound exhibits good bench stability and compatibility with standard purification protocols, making it well-suited for use in iterative synthesis campaigns targeting kinase inhibitors and other bioactive molecules.
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Lot numbers can be found on the outside label of a product: