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Structure of 1207176-24-6
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tert-Butyl 4-(bromomethyl)-4-fluoropiperidine-1-carboxylate delivers a reactive bromomethyl handle adjacent to a fluorinated piperidine scaffold, enabling site-specific functionalization in medicinal chemistry. The bench-stable, moisture-tolerant ester facilitates efficient coupling reactions under mild conditions, streamlining the synthesis of complex fluorinated heterocycles.
tert-Butyl 4-(bromomethyl)-4-fluoropiperidine-1-carboxylate serves as a versatile building block for the synthesis of fluorinated piperidine scaffolds. The bromomethyl group enables efficient nucleophilic substitution reactions, while the 4-fluoro substituent imparts enhanced metabolic stability and modulates electronic properties. The tert-butyl carbamate protection ensures compatibility with diverse reaction conditions, facilitating straightforward deprotection and functionalization. This reagent offers excellent bench stability and ease of purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and process 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 : 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: