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Structure of 1956434-67-5
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(oxazol-5-yl)propanoic acid features a chiral center flanked by a fluorenylmethoxycarbonyl (Fmoc) protecting group and a sterically constrained oxazol-5-yl side chain. This combination enables efficient incorporation into peptide synthesis workflows, offering enhanced solubility and stability under standard coupling conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(oxazol-5-yl)propanoic acid serves as a valuable chiral building block in peptide synthesis, enabling efficient incorporation of oxazol-5-yl functionality at the C-terminal position. The Fmoc group provides excellent stability and ease of removal under mild basic conditions, while the oxazol-5-yl side chain offers a robust heterocyclic moiety with proven utility in medicinal chemistry scaffolds. Its compatibility with standard coupling protocols and straightforward purification make it well-suited for both academic and industrial peptide 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: