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Structure of 934536-10-4
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tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate delivers a fluorinated piperidine scaffold with a readily manipulable amino group, enabling direct functionalization in medicinal chemistry. The tert-butyl carbamate protects the amine under standard conditions while maintaining compatibility with diverse transformations. This derivative supports efficient synthesis of bioactive compounds featuring constrained, electron-deficient heterocycles.
tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated piperidine scaffolds. The protected amine and fluorinated C3 position facilitate downstream functionalization via standard coupling, reduction, and electrophilic substitution reactions. Its bench-stable tert-butyl carbamate group simplifies purification and offers orthogonal reactivity, making it well-suited for iterative synthesis of bioactive molecules.
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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: