Product Data Sheet

2’,3’-Di-O-isopropylidene-4’-alpha-C-azidouridine

Catalog No. A56359

main product photo
2’,3’-Di-O-isopropylidene-4’-alpha-C-azidouridine is a uridine analog that serves as a valuable tool in the study of anticonvulsant and anxiolytic properties, with potential applications in developing antihypertensive agents. This compound features an azide group, enabling it to function as a click chemistry reagent through copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalized compounds, facilitating bioconjugation and tracer development in chemical biology.
Chemical Information
Catalog NumA56359
M. Wt325.28
FormulaC12H15N5O6
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.690271-27-3
Synonyms
SMILESO=C(NC1=O)C=CN1[C@H](O2)[C@H]3[C@H](OC(C)(C)O3)[C@]2(CO)N=[N+]=[N-]
Biological Activity
Description2’,3’-Di-O-isopropylidene-4’-alpha-C-azidouridine is a uridine analog that serves as a valuable tool in the study of anticonvulsant and anxiolytic properties, with potential applications in developing antihypertensive agents. This compound features an azide group, enabling it to function as a click chemistry reagent through copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalized compounds, facilitating bioconjugation and tracer development in chemical biology.
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SHIPPING AND STORAGE
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