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| Product | Description | |
|---|---|---|
| (2S,3S)-Fmoc-Abu(3-N3)-OH | A useful tool for the synthesis of branched, side-chain modified, cyclic peptides and peptide tools for click chemistry. The side-chain azido group is completely stable to piperidine and TFA, but can be readily converted to an amine on the solid phase or in solution by reduction with thiols or phosphines. Uses: Peptide synthesis. Additional or Alternative Names: (2S,3S)-Fmoc-Abu(3-N3)-OH, (2S,3S)-2-(Fmoc-amino)-3-azidobutanoic acid. Product Category: Amino Acids. CAS No. 131669-42-6. Mole weight: 366.37. Product ID: ACM131669426. Alfa Chemistry ISO 9001:2015 Certified. |  |
| (2S,3S)-(Fmoc-amino)-3-azidobutyric acid | Protected derivative for the synthesis of 2,3-diaminobutanoic acid containing peptides and also for click reactions. Synonyms: Fmoc-L-Abu(3S-N3)-OH; (2S,3S)-Fmoc-abu(3-n3)-oh; (2S,3S)-(Fmoc-amino)-3-azidobutyric acid; (2S,3S)-3-azido-2-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid. Grades: ≥ 99% (Assay by titration, HPLC, TLC). CAS No. 131669-42-6. Molecular formula: C19H18N4O4. Mole weight: 366.40. |  |
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