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Structure of 5001-26-3
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This benzylamine-substituted phenol features a strategically positioned amine-alkyl linker that enhances solubility and reactivity in synthetic transformations. The ortho-hydroxyl group enables coordination to metal catalysts, while the benzylamino methyl moiety provides a handle for further derivatization. Bench-stable under standard conditions, it integrates seamlessly into multistep synthesis workflows.
2-((Benzylamino)methyl)phenol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard condensation and cyclization protocols. Its pendant benzylamine and phenolic functionalities offer orthogonal reactivity for selective derivatization, while the molecule exhibits robust bench stability and straightforward purification—facilitating integration into multi-step synthetic sequences for API development.
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Lot numbers can be found on the outside label of a product: