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Structure of 1212176-33-4
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This chiral piperidine derivative features a protected amine and a ketone-functionalized ring, enabling direct incorporation into peptide synthesis workflows. The tert-butoxycarbonyl group ensures stability during manipulations, while the 4-oxo and carboxylic acid moieties provide dual handles for orthogonal coupling strategies in medicinal chemistry applications.
(R)-1-(tert-Butoxycarbonyl)-4-oxopiperidine-2-carboxylic acid serves as a versatile chiral building block in the synthesis of bioactive heterocycles and peptidomimetics. Its protected amine and ketone functionalities enable sequential transformations, including reductive amination and nucleophilic addition, with high stereocontrol. The tert-butyl carbamate group provides bench stability and facilitates straightforward deprotection under mild acidic conditions, enhancing utility in iterative 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 : H319
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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: