| Catalogue number: | PA 27 0031482 |
| Chemical name: | Fmoc-L-Lys(4-N3-Z)-OH |
CAS Number: |
1446511-14-3 |
| Category: | miscellaneous compounds,Antibody Drug Conjugate |
| Synonyms: | N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N6-(((4-azidobenzyl)oxy)carbonyl)-L-lysine; L-Lysine, N6-[[(4-azidophenyl)methoxy]carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-; N6-[[(4-Azidophenyl)methoxy]carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine; |
| Molecular form: | C29H29N5O6 |
| Appearance: | NA |
| Mol. Weight: | 543.58 |
| Storage: | 2-8°C Refrigerator |
| Shipping Conditions: | Ambient |
| Applications: | Fmoc-L-Lys(4-N3-Z)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Lys(4-N3-Z)-OH acts as Lysine building-block for SPPS containing an Azide moiety as a bioorthogonal ligation handle, an infrared probe and a photo-affinity reagent. It can be decaged by trans-cyclooctenols via a strain-promoted 1,3-dipolar cycloaddition[1][2]. Fmoc-L-Lys(4-N3-Z)-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. |
Fmoc-L-Lys(4-N3-Z)-OH
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