159496-13-6

Basic information

• Product Name: Adenosine-13C5
• Synonyms: Adenosine-13C5;1-(6-AMino-9H-purin-9-yl)-1-deoxy-β-D-ribofuranose-13C5;9-β-D-Ribofuranosyl-9H-purin-6-aMine-13C5;9-β-D-Ribofuranosyladenine-13C5;Adenine Riboside-13C5;Adenocard-13C5;Adenocor-13C5;Adenogesic-13C5
• CAS NO: 159496-13-6
• Molecular Formula: C513C5H13N5O4
• Molecular Weight: 272
• Product Categories: Bases & Related Reagents;Isotope Labelled Compounds;Nucleotides;Isotope Labelled Compounds, Nucleotides, Bases & Related Reagents
• Mol File: 159496-13-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 233-235°C (dec.)
• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: DMSO (Slightly), Methanol (Slightly, Sonicated), Water (Slightly, Sonicated)
• Stability: Hygroscopic
• CAS DataBase Reference: Adenosine-13C5(CAS DataBase Reference)
• NIST Chemistry Reference: Adenosine-13C5(159496-13-6)
• EPA Substance Registry System: Adenosine-13C5(159496-13-6)

Safety Data

• Hazardous Substances Data: 159496-13-6(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

Labelled nucleotide.

Upstream product

• 503173-75-9 ¹³C₅-1′, 2 ′-di-O-acetyl-3 ′ ,5 ′-di-O-benzoyl-β-D-ribofuranose 
• 503173-74-8 [ribose-13C5]-3,5-di-O-benzoyl-1,2-O-isopropylidene-α-D-ribofuranose 
• 238096-51-0 <1,2,3,4,5-13C5>-1,2-O-isopropylidene-α-D-ribofuranose 
• 503173-77-1 [ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)adenine 
• 66224-66-6 adenine 
• 159496-09-0 [13C5]-1,2-di-O-acetyl-3,5-di-O-benzoyl-α,β-D-ribofuranose 
• 159496-08-9 C₄⁽¹³⁾C₅H₁₆O₇S 

Relevant articles and documents

Chemical synthesis of 13C labeled anti-HIV nucleosides as mass-internal standards

Synthesis of [13C5]-labeled anti-HIV nucleosides, e.g. d4T, ddI, ddA, is described. The methodology used has been optimized due to the very high cost of the starting compound. The key step of this approach was the stereoselective dehomologation of 1,2:5,6-di-O-isopropylidene-3-oxo-α-D-glucofuranose (2) with periodic acid and sodium borohydride, which gave optically pure ribose derivative as the exclusive product. Nucleoside derivatives 6a-c were obtained from ribosylation of 5 with persilylated nucleobases under Vorbru?ggen conditions. Deoxygenation of 9a-c under Corey-Winter conditions afforded the desired labeled nucleoside analogues 12a-c.