5-Azidomethyl-2’,3’,5’-tri-O-benzoyl uridine is a thymidine analog designed for applications in DNA research. This compound exhibits insertional activity towards replicated DNA, facilitating the labeling of cells and tracking of DNA synthesis. As a versatile click chemistry reagent, it features an azide group that engages in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions, making it suitable for bioconjugation strategies involving alkyne, DBCO, or BCN functionalized molecules.
5-Azidomethyl-2’,3’,5’-tri-O-benzoyl uridine is a thymidine analog designed for applications in DNA research. This compound exhibits insertional activity towards replicated DNA, facilitating the labeling of cells and tracking of DNA synthesis. As a versatile click chemistry reagent, it features an azide group that engages in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions, making it suitable for bioconjugation strategies involving alkyne, DBCO, or BCN functionalized molecules.
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