CAS 39747-65-4
:L-Serine,N-[(1,1-dimethylethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester
Description:
L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester, with CAS number 39747-65-4, is a chemical compound that features a serine amino acid derivative. This compound is characterized by the presence of a pyrrolidine ring, which is a five-membered cyclic amine, and a carbonyl group that contributes to its reactivity. The dimethylethoxycarbonyl group serves as a protective moiety, enhancing the stability of the serine residue during synthetic processes. L-Serine itself is a non-essential amino acid important in protein synthesis and various metabolic pathways. The esterification of serine in this compound suggests potential applications in peptide synthesis or as an intermediate in organic synthesis. Its structural features may also influence its solubility, reactivity, and interaction with biological systems. Overall, this compound exemplifies the complexity of amino acid derivatives and their utility in chemical and pharmaceutical applications.
Formula:C12H18N2O7
Synonyms:- Carbamicacid, [2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-1-(hydroxymethyl)-2-oxoethyl]-, 1,1-dimethylethylester, (S)-
- N-(tert-Butyloxycarbonyl)-L-serine ester withN-hydroxysuccinimide
- Boc-Ser-OSu
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Found 4 products.
(S)-2,5-Dioxopyrrolidin-1-yl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate
CAS:(S)-2,5-Dioxopyrrolidin-1-yl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoatePurity:95%Molecular weight:302.28g/mol(S)-2,5-Dioxopyrrolidin-1-yl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate
CAS:Purity:95%Molecular weight:302.2829895Boc-L-serine N-hydroxysuccinimide ester
CAS:<p>Boc-L-serine N-hydroxysuccinimide ester is a chromatographic reagent that functions as an effective method for the synthesis of peptides. This reagent can be used in silylation reactions to introduce hydroxyl groups onto amino acid side chains. It also has a melting point of 210°C, and can be used to determine the sequence of peptides by optical spectroscopy. The result is a mobility shift in the spectrum of the peptide, which corresponds to a change in its sequence. The mobilities at different wavelengths are determined by nmr spectra. Boc-L-serine N-hydroxysuccinimide ester is most commonly used for the synthesis of peptides with masses corresponding to less than 10 kDa and with up to two amino acid residues per molecule.</p>Formula:C12H18N2O7Purity:Min. 95%Molecular weight:302.28 g/mol



