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Structure of 2306264-96-8
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6-Methylspiro[indoline-3,4'-piperidin]-2-one hydrochloride features a rigid spirocyclic scaffold with enhanced solubility and stability under standard conditions. The protonated piperidine nitrogen facilitates salt formation, improving handling and compatibility in synthetic workflows. This structural motif serves as a key intermediate in medicinal chemistry campaigns targeting CNS-directed therapeutics.
6-Methylspiro[indoline-3,4'-piperidin]-2-one hydrochloride serves as a versatile spirocyclic scaffold in medicinal chemistry, enabling efficient construction of complex heterocyclic architectures. Its stability, solubility in common organic solvents, and compatibility with standard functional group manipulations facilitate straightforward derivatization. The molecule functions effectively in peptide coupling, reductive amination, and transition-metal-catalyzed transformations, supporting rapid exploration of analogs for CNS-targeted therapeutics and kinase inhibitors.
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Lot numbers can be found on the outside label of a product: