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Structure of 172965-84-3
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a robust C-terminal carbamate linkage, enabling efficient coupling in solid-phase peptide synthesis. The fluoren-9-ylmethoxy carbonyl (Fmoc) group ensures high-yield deprotection under mild basic conditions, while the methylamino side chain provides enhanced solubility and reduced aggregation during chain assembly.
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)propanoic acid serves as a versatile protected amino acid building block, enabling efficient peptide synthesis via standard coupling protocols. The Fmoc-methylamino group offers high stability under basic conditions and facilitates rapid deprotection, while the propanoic acid side chain provides a well-defined functional handle for further diversification. Its bench-stable nature and compatibility with common purification methods make it ideal for iterative solid-phase and solution-phase synthesis 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-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: