279670-58-5

Basic information

• Product Name: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(4-methoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
• Synonyms: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(4-methoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
• CAS NO: 279670-58-5
• Molecular Weight: 484.466
• Mol File: 279670-58-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(4-methoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(4-methoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(279670-58-5)
• EPA Substance Registry System: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(4-methoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(279670-58-5)

Safety Data

• Hazardous Substances Data: 279670-58-5(Hazardous Substances Data)

Upstream product

• 5987-73-5 2',3',5'-O-triacetyl-6-chloroinosine 
• 5720-07-0 4-methoxyphenylboronic acid 
• 3181-38-2 2’,3’,5’-tri-O-acetylinosine 
• 58-63-9 inosine 

Relevant articles and documents

Synthesis and cytostatic activity of substituted 6-phenylpurine bases and nucleosides: Application of the Suzuki-Miyaura cross-coupling reactions of 6-chloropurine derivatives with phenylboronic acids

The Suzuki-Miyaura reaction of protected 6-chloropurine and 2-amino-6- chloropurine bases and nucleosides with substituted phenylboronic acids led to the corresponding protected 6-(substituted phenyl)purine derivatives 6-9. Their deprotection yielded a se

Fluoro, alkylsulfanyl, and alkylsulfonyl leaving groups in suzuki cross-coupling reactions of purine 2′-deoxynucleosides and nucleosides

(Chemical Equation Presented) Protected 2′-deoxynucleoside and nucleoside derivatives of 6-fluoropurine, 6-(3-methylbutyl)sulfanylpurine, and 6-(3-methylbutyl)ylsulfonylpurine undergo nickel- or palladium-mediated C-C cross-coupling with arylboronic acids