Cat#: CCR-0106
Fmoc-β-azido-Ala-OH
Synonyms (s): (S)-3-Azido-2-(Fmoc-amino)propionic acid, Fmoc-3-azido-L-alanine
Empirical Formula (Hill Notation): C18H16N4O4
Size: 250 mg
Product Introduction
| Molecular Weight | 352.34 |
| NACRES | NA.26 |
| CAS Number | 684270-46-0 |
| MDL Number | MFCD11052919 |
| PubChem Substance ID | 329763258 |
| Assay | ≥98.0% (HPLC) |
| Form | Lumps |
| Reaction Suitability | Reaction type: Fmoc solid-phase peptide synthesis; Reaction type: click chemistry |
| Smiles String | OC(=O)[C@H](CN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c3ccccc13 |
| InChI | 1S/C18H16N4O4/c19-22-20-9-16(17(23)24)21-18(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,21,25)(H,23,24)/t16-/m0/s1 |
| InChI key | ZITYCUDVCWLHPG-INIZCTEOSA-N |
| Storage Temp. | 2-8 °C |
Application
Fmoc-β-azido-Ala-OH chloride is a general N-terminal protected reagent used in the solid phase peptide synthesis. Azido group allows it to undergo copper-mediated click chemistry reactions.It can be used in:Synthesis of α-N-acetylgalactosamine (α-GalNAc) linked antifreeze glycopeptides (AFGPs).Synthesis of stimuli-responsive multifunctional peptide gatekeepers for drug delivery applications.Synthesis of triazole-linked glycopeptides via Cu(I)-catalyzed 1,3-dipolar cycloaddition (CuAAC).
Safety Information
| Storage Class Code | 13 - Non Combustible Solids |
| WGK | WGK 3 |
For research use only. Not for clinical use.
