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Structure of 913253-24-4
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-cyanobutanoic acid features a chiral center at the alpha position, enabling stereoselective incorporation into peptide sequences. The fluorenylmethyl carbamate (Fmoc) group provides orthogonal protection for amines, while the pendant nitrile imparts enhanced solubility and reactivity in solid-phase synthesis. This building block streamlines the assembly of complex peptides under standard conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-cyanobutanoic acid serves as a valuable chiral building block in peptide synthesis, enabling the incorporation of γ-cyanoalanine derivatives with high enantioselectivity. The Fmoc group provides excellent stability and ease of removal under mild basic conditions, while the nitrile functionality offers versatile downstream transformations. Its robust bench stability 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-H335
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Precautionary Statements : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: