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Structure of 278798-15-5
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tert-Butyl 4-(1H-pyrazol-4-yl)piperidine-1-carboxylate features a pyrazole-functionalized piperidine core with a bench-stable tert-butoxycarbonyl protecting group. This compound integrates readily into medicinal chemistry campaigns, enabling efficient access to bioactive heterocycles through straightforward deprotection. The electron-rich pyrazole moiety enhances target engagement in kinase and receptor modulation studies.
tert-Butyl 4-(1H-pyrazol-4-yl)piperidine-1-carboxylate serves as a versatile building block for medicinal chemistry, enabling efficient access to pyrazole-containing piperidine scaffolds. The tert-butyl carbamate group provides excellent bench stability and facile removal under mild acidic conditions, while the 1H-pyrazol-4-yl moiety offers a robust hydrogen-bonding pharmacophore. It functions effectively in standard coupling reactions and supports diversification via late-stage functionalization, making it ideal for high-throughput synthesis of bioactive molecules.
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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: