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Structure of 20289-27-4
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7-(Benzyloxy)-1H-indole serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through orthogonal functionalization. The benzyloxy group provides robust protection for the phenolic hydroxyl and can be selectively removed under mild conditions, facilitating downstream derivatization. Its stability under standard reaction protocols and compatibility with diverse coupling reactions make it a practical choice for synthesizing complex heterocyclic systems and API intermediates.
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Lot numbers can be found on the outside label of a product: