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Structure of 285996-72-7
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This fluorenylmethoxycarbonyl-protected tetrahydropyran carboxylic acid serves as a specialized amino acid surrogate in peptide synthesis. The C-terminal carbamate functionality enables orthogonal deprotection, while the fluoren-9-ylmethoxy carbonyl group ensures high coupling efficiency and minimal side reactions under standard conditions.
4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)tetrahydro-2H-pyran-4-carboxylic acid serves as a versatile protected amino acid building block, enabling efficient peptide coupling and heterocyclic scaffold construction. The Fmoc group provides excellent stability under basic conditions and facilitates straightforward deprotection, while the tetrahydropyran-4-carboxylic acid moiety offers a rigid, hydrophobic core suitable for medicinal chemistry applications. Its compatibility with standard solid-phase synthesis protocols and ease of purification make it a practical choice for complex molecule assembly.
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Lot numbers can be found on the outside label of a product: