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Structure of 321997-89-1
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This bench-stable piperidine derivative features a tert-butyl-protected amine and methyl ester functionalities, enabling straightforward deprotection and derivatization. The electron-rich nitrogen centers facilitate efficient coupling reactions, making it a robust scaffold for medicinal chemistry libraries and peptide mimetics.
1-tert-Butyl 4-methyl 4-aminopiperidine-1,4-dicarboxylate serves as a versatile building block in medicinal chemistry, enabling the construction of piperidine-based scaffolds common in bioactive molecules. The protected amine and ester functionalities offer orthogonal reactivity, facilitating selective transformations. Bench-stable and readily purified, it functions effectively in standard coupling, alkylation, and cyclization protocols for 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: