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*For research and further manufacturing use only, not for direct human use.
Structure of 846057-27-0
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This piperidine-based ketone features a hydroxymethyl group enabling direct functionalization or derivatization. The carbonyl moiety supports nucleophilic addition, while the pendant hydroxyl offers hydrogen-bonding capacity. Bench-stable and compatible with standard synthetic protocols, it serves as a versatile scaffold for medicinal chemistry campaigns requiring polar, nitrogen-rich motifs.
1-[4-(Hydroxymethyl)piperidin-1-yl]ethan-1-one serves as a versatile building block in medicinal chemistry, enabling the construction of piperidine-based scaffolds through subsequent functionalization. The pendant hydroxymethyl group facilitates derivatization via oxidation, protection, or coupling reactions, while the acetyl functionality provides a handle for selective transformations. Bench-stable and compatible with standard synthetic workflows, it supports efficient access to bioactive molecules in drug discovery programs.
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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
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: