34349-03-6

5-(Azidomethyl) arauridine Chemical Structure
34349-03-6

Chemical Structure

5-(Azidomethyl) arauridine

  • CAS No.: 34349-03-6
  • Formula:C10H13N5O6
  • Molecular Weight:299.24

IUPAC Name: 5-(azidomethyl)-1-((2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

InChIKey: ZAFBFGDCEFQDFD-JVZYCSMKSA-N

SMILES: O[C@@H]1[C@@H](O)[C@H](N2C=C(CN=[N+]=[N-])C(NC2=O)=O)O[C@@H]1CO

Biological Activity: 5-(Azidomethyl) arauridine is a thymidine analogue. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis[1]. 5-(Azidomethyl) arauridine 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.

Cat. No. Product Name Purity Description Pricing
HY-152523
5-(Azidomethyl) arauridine 5-(Azidomethyl) arauridine is a thymidine analogue. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis. 5-(Azidomethyl) arauridine 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.
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