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Structure of 1086392-24-6
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tert-Butyl 3-(aminomethyl)indoline-1-carboxylate features a protected amine and indoline scaffold, enabling direct incorporation into bioactive molecule synthesis. The tert-butyl carbamate group offers stability and convenient deprotection under mild acidic conditions. This building block integrates efficiently into peptidomimetics and kinase inhibitors, delivering enhanced solubility and metabolic resistance in drug discovery workflows.
tert-Butyl 3-(aminomethyl)indoline-1-carboxylate serves as a versatile building block for indoline-based scaffolds in medicinal chemistry. The protected amine and carboxylate functionalities enable sequential functionalization, while the tert-butyl group offers stability and ease of removal under mild acidic conditions. It facilitates efficient synthesis of bioactive indolines via standard coupling, reduction, or cyclization protocols.
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Lot numbers can be found on the outside label of a product: