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Structure of 214147-48-5
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1-(4-Aminopiperidin-1-yl)ethanone hydrochloride features a primary amine within a piperidine ring, enabling direct conjugation in bioconjugation workflows. The hydrochloride salt enhances solubility and stability under standard conditions, facilitating use in medicinal chemistry synthesis. This scaffold integrates readily into peptidomimetic and kinase inhibitor frameworks.
1-(4-Aminopiperidin-1-yl)ethanone hydrochloride serves as a versatile building block in medicinal chemistry, enabling rapid access to diverse heterocyclic scaffolds. Its amine functionality facilitates straightforward derivatization via acylation, alkylation, and reductive amination. The piperidine core provides favorable solubility and metabolic stability, while the hydrochloride salt enhances bench stability and ease of handling. This compound functions effectively in standard coupling protocols and supports efficient synthesis of kinase inhibitors and CNS-targeted candidates.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: