26182-58-1

Basic information

• Product Name: {(2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-3-[(hydroxy{[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl]methoxy}phosphoryl)oxy]tetrahydrofuran-2-yl}methyl dihydrogen phosphate (non-preferred name)
• CAS NO: 26182-58-1
• Molecular Formula: C₂₀H₂₇N₇O₁₃P₂
• Molecular Weight: 635.415
• Mol File: 26182-58-1.mol
• Article Data: 2

Chemical Properties

• Density: 2.12g/cm³
• Refractive Index: 1.829
• CAS DataBase Reference: {(2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-3-[(hydroxy{[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl]methoxy}phosphoryl)oxy]tetrahydrofuran-2-yl}methyl dihydrogen phosphate (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: {(2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-3-[(hydroxy{[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl]methoxy}phosphoryl)oxy]tetrahydrofuran-2-yl}methyl dihydrogen phosphate (non-preferred name)(26182-58-1)
• EPA Substance Registry System: {(2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-3-[(hydroxy{[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl]methoxy}phosphoryl)oxy]tetrahydrofuran-2-yl}methyl dihydrogen phosphate (non-preferred name)(26182-58-1)

Safety Data

• Hazardous Substances Data: 26182-58-1(Hazardous Substances Data)

Upstream product

• 4546-64-9 N⁶-benzoyldeoxyadenosine 5'-phosphate 
• 4304-30-7 3'-O-acetylthimidine-5'-phosphate 
• 90399-74-9 N-{9-[(2R,4S,5R)-4-Hydroxy-5-(6-oxo-6,7-dihydro-5H-5,7-diaza-6λ⁵-phospha-dibenzo[a,c]cyclohepten-6-yloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-6-yl}-benzamide 
• 90399-77-2 C₄₁H₄₁N₉O₁₃P₂ 

Relevant articles and documents

PROTECTION OF 5'-TERMINAL PHOSPHATE OF DEOXYRIBOOLIGONUCLEOTIDES BY USE OF o,o'-DIAMINOBIPHENYL

Cyclic phosphorodianilidate derivatives of nucleoside 5'-phosphates were prepared by use of triphenylphosphine and 2,2'-dipyridyl disulfide as condensing agent and used for the synthesis of oligodeoxyribonucleotides.Removal of the diamino group was remarkably accelerated by coaddition of AgOAc and acid anhydrides to the conventional system, iAmONO-pyridine-AcOH.