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Structure of 534602-47-6
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This piperidine derivative features a tert-butoxycarbonyl-protected amine and a methyl-substituted carboxylic acid, enabling direct incorporation into peptide synthesis workflows. The protected nitrogen facilitates efficient coupling reactions under standard conditions, while the sterically hindered methyl group enhances metabolic stability in bioactive molecule design.
1-(tert-Butoxycarbonyl)-3-methylpiperidine-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of piperidine-based scaffolds with defined stereochemistry. The Boc-protected amine and carboxylic acid functionality offer orthogonal reactivity for peptide coupling and subsequent deprotection. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient access to complex heterocyclic architectures in API 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-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: