This cysteine derivative carries a trityl-protected thiol and a methylated backbone carbon, enhancing steric control. Researchers use it in peptide cyclization studies and redox-sensitive constructs. The protective groups ensure selective reactivity at designated steps. Its configuration supports advanced synthetic strategies.
CAT No: R2114
CAS No:725728-43-8
Synonyms/Alias:N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-methyl-S-(triphenylmethyl)-L-cysteine;725728-43-8;Fmoc-alpha-Me-L-Cys(Trt)-OH;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-methyl-S-(triphenylmethyl)-L-cysteine;(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-(tritylthio)propanoic acid;(R)-Fmoc-2-amino-2-methyl-3-tritylsulfanyl-propionic acid;Fmoc-alpha-Me-Cys(Trt)-OH;MFCD30749166;Fmoc-(Me)Cys(Trt)-OH;Fmoc-beta-Me-Cys(Trt)-OH;SCHEMBL3435366;Fmoc-S-trityl-alpha-Me-L-cysteine;N-Fmoc-2-methyl-S-trityl-L-cysteine;CS-0160399;D81095;(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-3-tritylsulfanylpropanoic acid;(2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2-methyl-3-[(triphenylmethyl)sulfanyl]propanoic acid;
2. TMEM16F and dynamins control expansive plasma membrane reservoirs
5. SERS spectrum of the peptide thymosin‐β4 obtained with Ag nanorod substrate
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