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Structure of 63845-28-3
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This piperidine-based scaffold features a benzyloxycarbonyl-protected amine and a pendant acetic acid group, enabling direct incorporation into peptide synthesis workflows. The Cbz moiety provides orthogonal protection, while the carboxylic acid serves as a reactive handle for coupling reactions under standard conditions.
2-(1-((Benzyloxy)carbonyl)piperidin-4-yl)acetic acid serves as a versatile building block for the synthesis of piperidine-containing pharmaceuticals and bioactive heterocycles. The benzyl carbamate (Cbz) group provides orthogonal protection for the piperidine nitrogen, enabling selective deprotection during late-stage functionalization. The pendant acetic acid moiety facilitates conjugation via amide bond formation or metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with standard peptide and medicinal chemistry workflows make it ideal for modular library synthesis and 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: