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Structure of 2044709-77-3
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral (R)-configuration at the alpha carbon, enabling stereoselective peptide synthesis. The C-terminal carboxylic acid group and N-terminal Fmoc moiety facilitate efficient coupling reactions, while the tert-butoxycarbonyl-methylamino side chain provides a stable, orthogonal protecting group for selective deprotection. Designed for solid-phase peptide synthesis, this reagent ensures high yield and purity in complex sequence assembly.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-((tert-butoxycarbonyl)(methyl)amino)hexanoic acid serves as a versatile chiral building block for peptide synthesis, enabling efficient N-terminal protection and side-chain modulation. The Fmoc group ensures orthogonal deprotection under mild basic conditions, while the Boc-methyl amino functionality provides a stable, selectively removable amine handle. Its bench-stable, crystalline nature facilitates straightforward purification and compatibility with standard coupling protocols in solid-phase and solution-phase workflows.
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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: