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Structure of 351410-32-7
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This piperidine-based acetic acid derivative features a tert-butoxycarbonyl-protected amine and a pendant carboxylic acid, enabling direct incorporation into peptide synthesis. The protected nitrogen facilitates efficient coupling reactions under standard conditions, while the aliphatic backbone provides solubility and stability in common organic solvents.
2-[(2R)-1-[(tert-butoxy)carbonyl]piperidin-2-yl]acetic acid serves as a versatile building block for synthesizing bioactive heterocycles and peptidomimetics. Its pendant carboxylic acid enables straightforward coupling reactions, while the Boc-protected piperidine moiety offers stability and orthogonal functionality. The molecule facilitates efficient access to constrained scaffolds relevant in medicinal chemistry, with excellent bench stability and compatibility in standard peptide and combinatorial synthesis workflows.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: