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Structure of 2044711-09-1
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This (R)-configured fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered trityl group and a labile carbamate linkage, enabling efficient incorporation into peptide chains under mild deprotection conditions. The electron-rich fluoren-9-yl moiety facilitates UV detection during synthesis, while the methylamino functionality supports selective coupling reactions. This robust scaffold delivers high-purity peptides with minimal epimerization.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-oxo-4-(tritylamino)butanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient N-terminal protection and side-chain functionalization. The fluorenylmethoxycarbonyl (Fmoc) group ensures orthogonal deprotection under mild basic conditions, while the trityl-protected amine provides steric shielding and enhanced solubility. Its bench-stable nature and compatibility with standard coupling protocols facilitate reliable incorporation into complex peptide scaffolds.
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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: