| Catalogue number: | PA 27 0032372 |
| Chemical name: | N3-L-Dap(Boc)-OH |
CAS Number: |
1932432-15-9 |
| Category: | miscellaneous compounds,Antibody Drug Conjugate |
| Synonyms: | (S)-2-Azido-3-((tert-butoxycarbonyl)amino)propanoic Acid; Propanoic acid, 2-azido-3-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-; (2S)-2-Azido-3-[[(1,1-dimethylethoxy)carbonyl]amino]propanoic Acid; |
| Molecular form: | C8H14N4O4 |
| Appearance: | NA |
| Mol. Weight: | 230.22 |
| Storage: | 2-8°C Refrigerator |
| Shipping Conditions: | Ambient |
| Applications: | N3-L-Dap(Boc)-OH is a click chemistry reagent containing an azide group. Click chemistry is a powerful chemical reaction with excellent bioorthogonality features: biocompatible, rapid and highly specific in biological environments[1]. N3-L-Dap(Boc)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups |
N3-L-Dap(Boc)-OH
N3-L-Dap(Boc)-OH
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