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Structure of 368866-09-5
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This fluorenylmethoxycarbonyl-protected piperidine derivative features a sterically hindered, bench-stable amino acid scaffold ideal for solid-phase peptide synthesis. The C-terminal carboxylic acid group enables efficient coupling, while the fluorenylmethoxycarbonyl moiety provides orthogonal protection and clean deprotection under mild basic conditions.
4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)piperidine-4-carboxylic acid hydrochloride serves as a protected amino acid building block for peptide synthesis, enabling efficient N-terminal capping and side-chain compatibility in solid-phase and solution-phase workflows. The Fmoc group provides excellent stability under basic conditions and facilitates clean deprotection with piperidine. Its hydrochloride salt enhances solubility and handling, while the piperidine-4-carboxylic acid scaffold offers versatility in constructing cyclic peptides and heterocyclic scaffolds relevant to medicinal chemistry.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: