N-alpha-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine carries a heavily substituted aromatic thioether installed on cysteine. The modification stabilizes sulfur reactivity and alters redox behavior. Researchers employ it in cyclic peptide construction and controlled disulfide modeling. Its protections allow selective downstream transformations.
CAT No: R2145
CAS No:1403834-74-1
Synonyms/Alias:Fmoc-Cys(STmp)-OH;1403834-74-1;(2R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-[(2,4,6-trimethoxyphenyl)disulfanyl]propanoic acid;N-alpha-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine;N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-((2,4,6-trimethoxyphenyl)thio)-L-cysteine;Fmoc-L-Cys(Stmp)-OH;MFCD27957369;AKOS037645081;AS-56905;DA-63511;Fmoc-Cys(STmp)-OH (Non-Animal Origin);HY-134852;CS-0159827;F72597;(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-[(2,4,6-trimethoxyphenyl)disulfanyl]propanoic acid;(2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-[(2,4,6-trimethoxyphenyl)disulfanyl]propanoic acid;867-072-0;
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