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Structure of 159275-17-9
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Benzyl 4-(bromomethyl)piperidine-1-carboxylate features a reactive bromomethyl group enabling efficient alkylation and coupling reactions. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences for bioactive molecule construction, particularly in medicinal chemistry applications requiring piperidine scaffolds.
Benzyl 4-(bromomethyl)piperidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient construction of piperidine-based scaffolds. The bromomethyl group facilitates nucleophilic substitution reactions, while the benzyl ester provides orthogonal protection and ease of removal under standard hydrogenolysis conditions. Its stability and compatibility with diverse functional groups make it well-suited for iterative synthesis workflows 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 : 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: