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Structure of 507472-25-5
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-nitrophenyl)propanoic acid is a chiral building block featuring a fluorenylmethoxycarbonyl (Fmoc) protected amino group and a para-nitro-substituted phenyl moiety. This configuration enables direct incorporation into peptide synthesis workflows, where the Fmoc group facilitates efficient deprotection under mild basic conditions. The electron-deficient nitroaryl side chain enhances reactivity in coupling reactions and contributes to structural rigidity, improving stereochemical fidelity during sequence assembly.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-nitrophenyl)propanoic acid serves as a robust chiral building block for peptide synthesis, leveraging the orthogonal stability of the Fmoc group and the functional group tolerance of the ortho-nitrophenyl moiety. Its bench-stable nature and compatibility with standard coupling protocols enable efficient access to complex peptidomimetics and heterocyclic scaffolds in medicinal chemistry 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: