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| | N3-L-Lys(Fmoc)-OH Basic information |
| Product Name: | N3-L-Lys(Fmoc)-OH | | Synonyms: | (S)-(-)-2-Azido-6-(Fmoc-amino)hexanoic acid;N3-L-Lys(Fmoc)-OH;Nα-Azido-Nε-Fmoc-L-Lysine≥ 99% (HPLC);Na-Azido-Ne-Fmoc-L-Lysine;Nα-Azido-Nε-Fmoc-L-Lysine;N3-Lys(Fmoc) | | CAS: | 473430-12-5 | | MF: | C21H22N4O4 | | MW: | 394.43 | | EINECS: | | | Product Categories: | | | Mol File: | 473430-12-5.mol |  |
| | N3-L-Lys(Fmoc)-OH Chemical Properties |
| | N3-L-Lys(Fmoc)-OH Usage And Synthesis |
| Chemical Properties | White crystallilne powder | | Uses | N3-L-Lys(Fmoc)-OH is a click chemistry reagent containing an azide group[1]. N3-L-Lys(Fmoc)-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. | | References | [1] Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789. DOI:10.1080/17460441.2019.1614910 |
| | N3-L-Lys(Fmoc)-OH Preparation Products And Raw materials |
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