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Structure of 1260612-08-5
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This chiral piperidine derivative features a bench-stable tert-butyl carbamate protecting group and a fluorinated ring system, enabling direct incorporation into complex scaffolds. The (3R,4R) stereochemistry ensures predictable diastereoselective transformations in medicinal chemistry workflows.
(3R,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 fluorine substituent enable selective functionalization, while the tert-butyl carbamate group offers stability and ease of removal under mild acidic conditions. This compound facilitates efficient access to complex nitrogen-containing heterocycles and is well-suited for iterative synthesis workflows requiring orthogonal reactivity and bench-stable intermediates.
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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: