Product Information
- (Boc-Cys-OH)
- (Boc-Cys-OH)2
- (Boc-Cys-OH)2 (Disulfide bond)
- <span class="text-smallcaps">L</span>-Cystine, N,N′-bis[(1,1-dimethylethoxy)carbonyl]-
- Cystine, N,N′-dicarboxy-, N,N′-di-tert-butyl ester
- Cystine, N,N′-dicarboxy-, N,N′-di-tert-butyl ester, <span class="text-smallcaps">L</span>-
- N,N'-Bis-Boc-L-cystine
- N,N'-bis(tert-butoxycarbonyl)-L-cystine
- N,N'-bis(tert-butoxycarbonyl)cystine
- N,N-bis(T-boc)-L-cystine
- See more synonyms
- N,N′-Bis(tert-butoxycarbonyl)-<span class="text-smallcaps">L</span>-cysteine
- N,N′-Bis(tert-butoxycarbonyl)-<span class="text-smallcaps">L</span>-cystine
- N,N′-Bis[(1,1-dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-cystine
- N,N′-Di(tert-butoxycarbonyl)-<span class="text-smallcaps">L</span>-cystine
- N,N′-Di-BOC-<span class="text-smallcaps">L</span>-cystine
- NSC 164046
Tai et al. could obtain asymmetric cystine peptides from (Boc-Cys-OH)₂ by enzymatic catalysis with immobilized papain. Oxidation of Boc-cystine with hydrogen peroxide in the presence of Na wolframate yielded the sodium salt of Boc-cysteic acid. Boc cystine benzyl ester was used as educt for obtaining S-isoacyl dipeptide building blocks.
Chemical properties
Technical inquiry about: 01-4001680 (Boc-Cys-OH)₂
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