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Structure of 1350629-55-8
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This chiral piperidine amine features a fluorinated stereocenter and a methylated nitrogen, enhancing metabolic stability and membrane permeability. The (3S,4R) configuration ensures optimal binding affinity in target-directed applications. Designed for synthetic efficiency, it integrates readily into bioactive scaffolds under standard conditions.
(3S,4R)-3-Fluoro-1-methylpiperidin-4-amine serves as a versatile chiral building block in medicinal chemistry, enabling the construction of fluorinated piperidine scaffolds prevalent in bioactive molecules. Its defined stereochemistry and functional group pattern facilitate predictable reactivity in amide coupling, alkylation, and cyclization processes. The compound exhibits good bench stability and compatibility with standard purification methods, supporting efficient integration into multi-step synthetic sequences for drug discovery applications.
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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: