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Structure of 1158319-57-3
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1-(3-Aminopiperidin-1-yl)ethan-1-one hydrochloride features a reactive ketone group flanked by a primary amine on a piperidine ring, enabling direct conjugation in synthetic workflows. The hydrochloride salt enhances solubility and stability under standard conditions, facilitating efficient incorporation into pharmaceutical intermediates and bioconjugation strategies.
1-(3-Aminopiperidin-1-yl)ethan-1-one hydrochloride serves as a versatile building block for medicinal chemistry, enabling rapid access to substituted piperidinone scaffolds. The amine functionality facilitates conjugation via acylation or reductive amination, while the ketone group supports nucleophilic addition and heterocycle formation. Its crystalline hydrochloride salt ensures bench stability, ease of handling, and straightforward purification—ideal for iterative synthesis campaigns in API development.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: