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Structure of 1197020-22-6
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)heptanoic acid is a chiral, bench-stable amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This robust, moisture-tolerant building block integrates seamlessly into peptide synthesis workflows, enabling efficient N-terminal protection and selective coupling in solid-phase and solution-phase strategies.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)heptanoic acid serves as a valuable chiral building block in peptide synthesis, offering high stereoselectivity and bench stability. The Fmoc group enables orthogonal protection of the amine, facilitating efficient coupling reactions under standard conditions. Its aliphatic side chain provides structural diversity for peptidomimetic design, while the carboxylic acid functionality supports direct conjugation or further derivatization in modular synthetic sequences.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: