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Structure of 109486-01-3
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1-(Prop-2-enoyl)piperidine-4-carboxylic acid features a conjugated enamide linkage that enhances reactivity in cycloaddition and condensation processes. The piperidine core provides a rigid, nitrogen-rich scaffold ideal for molecular scaffolding in medicinal chemistry. This compound integrates readily into complex heterocycles under mild conditions.
1-(Prop-2-enoyl)piperidine-4-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted piperidine scaffolds via Michael addition or cycloaddition protocols. The α,β-unsaturated enamide functionality facilitates conjugate addition reactions with nucleophiles, while the carboxylic acid group supports direct derivatization or coupling. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry campaigns requiring rapid structural diversification.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: