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Structure of 3569-21-9
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This indole-derived alcohol features a flexible propyl chain linking the aromatic indole core to a primary hydroxyl group. The moiety integrates readily into bioactive scaffolds, offering polarity and hydrogen-bonding capacity for medicinal chemistry applications. Bench-stable and moisture-tolerant, it serves as a direct handle for derivatization in synthetic campaigns.
3-(1H-Indol-3-yl)propan-1-ol serves as a versatile building block for indole-based scaffolds, enabling efficient incorporation into bioactive molecules. Its primary alcohol functionality facilitates straightforward derivatization via esterification, etherification, and oxidation to aldehyde. The molecule exhibits good bench stability and compatibility with standard synthetic protocols, supporting its use in medicinal chemistry campaigns targeting CNS agents and kinase inhibitors.
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Lot numbers can be found on the outside label of a product: