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Structure of 220498-02-2
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid features a chiral, bench-stable backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct incorporation into peptide synthesis workflows. The pendant phenyl moiety imparts enhanced solubility and structural rigidity, facilitating efficient coupling reactions under standard conditions.
(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid serves as a robust chiral building block for peptide synthesis, offering high stereochemical integrity and bench stability. The Fmoc group enables orthogonal protection, facilitating efficient deprotection under mild basic conditions. Its phenyl-substituted aliphatic side chain provides structural rigidity and enhances compatibility with standard coupling protocols, making it ideal for the synthesis of complex peptide architectures 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: