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Structure of 1359944-91-4
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tert-Butyl 4-bromo-3-fluoropiperidine-1-carboxylate features a sterically hindered piperidine core with complementary bromo and fluorine substituents enabling selective functionalization. This bench-stable intermediate facilitates the construction of complex nitrogen heterocycles in medicinal chemistry, particularly for targeted kinase inhibitors and CNS-active compounds.
tert-Butyl 4-bromo-3-fluoropiperidine-1-carboxylate serves as a versatile building block for the synthesis of fluorinated piperidine scaffolds prevalent in medicinal chemistry. The molecule combines a stable tert-butyl carbamate protecting group with strategically positioned bromo and fluoro substituents, enabling orthogonal functionalization via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient access to complex heterocyclic architectures used in 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: