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Structure of 250384-77-1
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hexanedioic acid features a fluorenylmethoxycarbonyl (Fmoc) protecting group coupled with a chiral, electron-rich hexanedioic acid backbone. This configuration enables reliable incorporation into peptide synthesis workflows, where the Fmoc moiety provides orthogonal deprotection under mild basic conditions. The molecule’s bench-stable, moisture-tolerant nature supports consistent handling in standard laboratory settings.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hexanedioic acid serves as a valuable chiral building block in peptide synthesis, offering orthogonal protection for both amine and carboxylic acid functionalities. The Fmoc group enables mild deprotection under basic conditions, while the pendant glutaric acid side chain provides a versatile handle for further functionalization. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for solid-phase and solution-phase peptide assembly.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: