N-alpha-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine

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.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
N-alpha-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine(CAS 1403834-74-1)

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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M.F/Formula
C27H27NO7S2
M.W/Mr.
541.6
InChI
InChI=1S/C27H27NO7S2/c1-32-16-12-23(33-2)25(24(13-16)34-3)37-36-15-22(26(29)30)28-27(31)35-14-21-19-10-6-4-8-17(19)18-9-5-7-11-20(18)21/h4-13,21-22H,14-15H2,1-3H3,(H,28,31)(H,29,30)/t22-/m0/s1
InChI Key
GADCBXMSWHDNAU-QFIPXVFZSA-N

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