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Structure of 406212-48-4
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tert-Butyl 3-(hydroxymethyl)-3-methylpiperidine-1-carboxylate delivers a sterically hindered piperidine scaffold with a pendant hydroxymethyl group, enabling direct functionalization or oxidation to aldehyde intermediates. This bench-stable building block integrates readily into medicinal chemistry campaigns requiring constrained nitrogen heterocycles with tunable polarity and solubility.
tert-Butyl 3-(hydroxymethyl)-3-methylpiperidine-1-carboxylate serves as a versatile scaffold for the synthesis of piperidine-based bioactive molecules, enabling efficient access to functionalized heterocycles. The hydroxymethyl group facilitates selective oxidation, protection, or derivatization, while the tert-butyl carbamate provides orthogonal protection compatible with diverse reaction conditions. Its bench-stable nature and ease of purification support scalable applications 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: