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Structure of 908847-01-8
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(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid features a chiral α-amino acid scaffold bearing a fluorenylmethoxycarbonyl (Fmoc) protecting group and a 6-fluoroindole side chain. This configuration enables direct incorporation into peptide synthesis workflows, offering enhanced solubility and stability under standard coupling conditions. The electron-deficient indole ring supports efficient amide bond formation, streamlining the assembly of complex bioactive sequences.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid serves as a valuable chiral building block for the synthesis of peptide-like scaffolds and bioactive heterocycles. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability and ease of removal under mild basic conditions, enabling efficient peptide elongation. The 6-fluoroindole moiety imparts enhanced metabolic stability and tunable electronic properties, making this compound particularly useful in medicinal chemistry campaigns targeting CNS-active molecules and kinase inhibitors.
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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: