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Structure of 193693-68-4
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(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidine-3-carboxylic acid is a chiral building block featuring a fluorenylmethoxycarbonyl (Fmoc) protected piperidine-3-carboxylic acid moiety. This derivative enables site-specific incorporation into peptide chains during solid-phase synthesis, offering enhanced solubility and stability under standard conditions. The Fmoc group facilitates orthogonal deprotection, streamlining the assembly of complex peptides with minimal side reactions.
(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidine-3-carboxylic acid serves as a key chiral building block in peptide synthesis, enabling efficient N-terminal protection of piperidine-based amino acids. The Fmoc group ensures high stability under basic conditions and facilitates straightforward removal via mild base treatment. Its well-defined stereochemistry and compatibility with standard coupling protocols make it ideal for constructing complex peptidomimetics and heterocyclic scaffolds in medicinal chemistry 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-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: