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Structure of 798576-99-5
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a bifunctional side chain enabling dual conjugation. The C-terminal carboxyl group facilitates coupling reactions, while the N-terminal Fmoc moiety ensures stable protection during synthesis. Designed for efficient incorporation into peptide chains under standard conditions.
4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-carboxyethyl)heptanedioic acid serves as a protected amino acid building block for the synthesis of peptide conjugates and complex heterocyclic scaffolds. The Fmoc group enables orthogonal deprotection under mild basic conditions, while the bis-carboxylic acid functionality supports efficient coupling reactions and metal chelation. Its bench-stable nature and compatibility with standard peptide synthesis workflows make it ideal for iterative solid-phase and solution-phase applications.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: