CAS 473278-54-5
:2-amino-9-[(2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)tetrahydrofuran-2-yl]-1H-purin-6-one
Description:
2-amino-9-[(2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)tetrahydrofuran-2-yl]-1H-purin-6-one, with CAS number 473278-54-5, is a purine derivative characterized by its complex structure that includes both amino and hydroxyl functional groups. This compound features a purine base, which is a key component of nucleic acids, and a sugar moiety derived from tetrahydrofuran, indicating its potential role in biological systems, particularly in nucleoside analogs. The presence of a methoxyethoxy group suggests enhanced solubility and stability, which may influence its pharmacological properties. The stereochemistry indicated by the (2R,3S,4S,5R) configuration is crucial for its biological activity, as it can affect interactions with enzymes and receptors. Overall, this compound may exhibit interesting biochemical properties, making it a candidate for further research in medicinal chemistry and drug development, particularly in the context of antiviral or anticancer therapies.
Formula:C13H19N5O6
InChI:InChI=1/C13H19N5O6/c1-22-2-3-23-9-8(20)6(4-19)24-12(9)18-5-15-7-10(18)16-13(14)17-11(7)21/h5-6,8-9,12,19-20H,2-4H2,1H3,(H3,14,16,17,21)/t6-,8+,9+,12-/m1/s1
InChI key:DLLBJSLIKOKFHE-WOUKDFQISA-N
SMILES:COCCO[C@@H]1[C@@H]([C@H](O[C@H]1N2C=NC3=C2N=C(NC3=O)N)CO)O
Synonyms:- 2'-O-(2-methoxyethyl)-guanosine
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2'-O-(2-Methoxyethyl)-guanosine
CAS:Formula:C13H19N5O6Purity:98%Color and Shape:SolidMolecular weight:341.31992-Amino-9-((2R,3R,4R,5R)-4-Hydroxy-5-(Hydroxymethyl)-3-(2-Methoxyethoxy)Tetrahydrofuran-2-Yl)-3H-Purin-6(9H)-One
CAS:2-Amino-9-((2R,3R,4R,5R)-4-Hydroxy-5-(Hydroxymethyl)-3-(2-Methoxyethoxy)Tetrahydrofuran-2-Yl)-3H-Purin-6(9H)-OneFormula:C13H19N5O6Purity:97%Molecular weight:341.322'-O-(2-Methoxyethyl)guanosine
CAS:2'-O-(2-Methoxyethyl)guanosine is a guanosine derivative isolated from the reaction of 2-aminoadenosine with methylsulfonyl chloride. This compound has been shown to react with aromatic hydrocarbons to form a reagent that is useful for the alkylation of nucleophilic groups in organic synthesis.Formula:C13H19N5O6Purity:Min. 95%Color and Shape:PowderMolecular weight:341.32 g/mol2′-O-(2-Methoxyethyl)-guanosine
CAS:Formula:C13H19N5O6Purity:98%Color and Shape:LiquidMolecular weight:341.1342′-O-(2-Methoxyethyl)guanosine
CAS:2-Amino-9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)tetrahydrofuran-2-yl)-3H-purin-6(9H)-oneFormula:C13H19N5O6Purity:97%Molecular weight:341.322'-O-(2-Methoxyethyl)guanosine
CAS:Controlled ProductFormula:C13H19N5O6Color and Shape:NeatMolecular weight:341.32





