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Structure of 10043-37-5
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This α,β-unsaturated ketone features a piperidinyl substituent that enhances solubility and reactivity in nucleophilic addition reactions. The conjugated enone system enables efficient Michael additions and Diels-Alder cycloadditions under mild conditions. Bench-stable and moisture-tolerant, it serves as a key building block for bioactive heterocycles and pharmaceutical intermediates.
1-(Piperidin-1-yl)prop-2-en-1-one serves as a versatile α,β-unsaturated carbonyl building block, enabling Michael additions and conjugate functionalizations under mild conditions. Its enone moiety exhibits high reactivity in nucleophilic addition reactions, particularly with amines and thiols, facilitating the construction of complex heterocyclic scaffolds. The piperidine group enhances solubility and provides a handle for further derivatization, while the molecule demonstrates bench stability and ease of purification—key attributes for iterative synthesis 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: