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Structure of 907544-20-1
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This chiral piperidine derivative features a tert-butyl carbamate-protected amine and a fluorine substituent at the 3-position, enabling selective incorporation into bioactive molecules. The (3S,4R) stereochemistry ensures precise spatial orientation for downstream applications in medicinal chemistry and peptide synthesis. Bench-stable and moisture-tolerant, it integrates seamlessly into complex molecule assembly workflows.
(3S,4R)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate serves as a stereochemically defined building block for fluorinated piperidine scaffolds prevalent in medicinal chemistry. The protected amine and fluorinated C3 position enable selective functionalization, facilitating downstream derivatization via nucleophilic substitution or reductive amination. Bench-stable and readily purified by chromatography, it functions effectively in peptide coupling, transition-metal-catalyzed cross-coupling, and heterocycle construction workflows.
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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-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P312-P337+P313-P363-P501
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Lot numbers can be found on the outside label of a product: