1610617-30-5

Basic information

• Product Name: 6-((1-(dimethylamino)ethylidene)amino)-9-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-2-yl diphenylcarbamate
• Synonyms: 6-((1-(dimethylamino)ethylidene)amino)-9-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-2-yl diphenylcarbamate
• CAS NO: 1610617-30-5
• Molecular Weight: 587.635
• Mol File: 1610617-30-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-((1-(dimethylamino)ethylidene)amino)-9-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-2-yl diphenylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: 6-((1-(dimethylamino)ethylidene)amino)-9-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-2-yl diphenylcarbamate(1610617-30-5)
• EPA Substance Registry System: 6-((1-(dimethylamino)ethylidene)amino)-9-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-2-yl diphenylcarbamate(1610617-30-5)

Safety Data

• Hazardous Substances Data: 1610617-30-5(Hazardous Substances Data)

Upstream product

• 1610617-29-2 N'-(9-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-2-oxo-2,9-dihydro-1H-purin-6-yl)-N,N-dimethylacetimidamide 
• 83-01-2 diphenylcarbamic chloride 
• 1818-71-9 1,2-dihydro-2-oxoadenosine 

Downstream Products

• 1610617-32-7 C₃₆H₄₂N₁₀O₇ 
• 1610617-40-7 C₄₇H₅₈N₁₀O₁₁ 

Relevant articles and documents

Modular construction of dynamic nucleodendrimers

Isoguanosine-containing dendritic small molecules self-assemble into decameric nucleodendrimers as observed by 1D NMR spectroscopy, 2D DOSY, and mass spectrometry. In particular, apolar building blocks readily form pentameric structures in acetonitrile while the presence of alkali metals promotes the formation of stable decameric assemblies with a preference for cesium ions. Remarkably, co-incubation of guanosine and isoguanosine-containing nucleodendrons results in the formation of decameric structures in absence of added salts. Further analysis of the mixture indicated that guanosine derivatives facilitate the formation, but are not involved in decameric structures; a process reminiscent of molecular crowding. This molecular system provides a powerful canvas for the rapid and modular assembly of polyfunctional dendritic macromolecules.