85110-26-5

Basic information

• Product Name: 6-(phenylethynyl)-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine
• Synonyms: 6-(phenylethynyl)-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine
• CAS NO: 85110-26-5
• Molecular Weight: 478.461
• Mol File: 85110-26-5.mol

Chemical Properties

• CAS DataBase Reference: 6-(phenylethynyl)-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(phenylethynyl)-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine(85110-26-5)
• EPA Substance Registry System: 6-(phenylethynyl)-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine(85110-26-5)

Safety Data

• Hazardous Substances Data: 85110-26-5(Hazardous Substances Data)

Upstream product

• 5987-73-5 2',3',5'-O-triacetyl-6-chloroinosine 
• 536-74-3 phenylacetylene 

Downstream Products

• 868738-70-9 6-(pentaphenylphenyl)-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine 
• 916346-29-7 6-[6-phenyl-2-cyano-2-(carboethoxy)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine 
• 916346-30-0 6-[6-phenyl-2,3-dihydro-2-tosyl-1H-isoindol-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine 
• 916346-28-6 6-[6-phenyl-2-acetyl-2-(carboxyethyl)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine 
• 528570-73-2 6-(6-phenyl-1,3-dihydroisobenzofuran-5-yl)-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine 

Relevant articles and documents

Preparation of highly substituted 6-arylpurine ribonucleosides by Ni-catalyzed cyclotrimerization. Scope of the reaction

Transition metal complex catalyzed cocyclotrimerization of protected alkynylpurine ribonucleosides 1 with various diynes 2 gave rise to a series of 6-arylpurine nucleosides 3 that were further deprotected to free nucleosides 4. Generally, the best yields

Novel method for preparation of highly substituted 6-arylpurines by reactions of 6-alkynylpurines with zirconacyclopentadienes

Reactions of various zirconacyclopentadienes bearing alkyl and aryl groups with 6-alkynyl-purines in the presence of NiBr2(PPh3) 2 afforded the corresponding 6-arylpurines with highly hydrophobic aryl moieties in low to mo