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Structure of 1217482-47-7
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)hexanoic acid features a chiral, bench-stable amino acid derivative with a fluorenylmethoxycarbonyl (Fmoc) protecting group. This configuration enables direct incorporation into peptide synthesis workflows, where the methylated amine prevents undesired side reactions while maintaining compatibility with standard coupling conditions.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)hexanoic acid serves as a valuable chiral building block in peptide synthesis, enabling efficient Nα-alkylation and side-chain functionalization. The Fmoc-methylamino handle provides excellent stability and orthogonal deprotection compatibility, while the (R)-configured hexanoic acid backbone supports diverse coupling reactions. Its bench-stable nature and clean purification profile facilitate scalable synthesis of complex peptidomimetics and bioactive 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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: