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Home  > Life Science  > DNA/RNA  > Nucleosides & Nucleotides  > (2R,3R,4S,5R)-2-(6-((3-Hydroxybenzyl)amino)-9h-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

AD66339

110505-76-5 | (2R,3R,4S,5R)-2-(6-((3-Hydroxybenzyl)amino)-9h-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

Packsize Purity Availability Price Discounted Price    Quantity
25mg 97% 2 weeks $41.00 $29.00 -   +
100mg 97% 2 weeks $75.00 $53.00 -   +
250mg 97% 2 weeks $144.00 $101.00 -   +
1g 97% 2 weeks $398.00 $279.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD66339
Chemical Name: (2R,3R,4S,5R)-2-(6-((3-Hydroxybenzyl)amino)-9h-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
CAS Number: 110505-76-5
Molecular Formula: C17H19N5O5
Molecular Weight: 373.3633
MDL Number: MFCD28343180
SMILES: OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1ncnc2NCc1cccc(c1)O

 

Upstream Synthesis Route
  • The compound (2R,3R,4S,5R)-2-(6-((3-Hydroxybenzyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol, or $name$, is commonly utilized in chemical synthesis due to its unique structural features and functional groups. In organic chemistry, this compound serves as a versatile building block for the construction of nucleoside analogs and pharmaceutical intermediates. Its hydroxyl groups can participate in various reactions such as esterification, ether formation, and glycosidic bond formation, enabling the synthesis of diverse molecular structures. Additionally, the purine moiety in $name$ offers potential for designing nucleotide analogs and antiviral agents through selective modifications. Its tetrahydrofuran ring provides stability and rigidity to the compound, making it an attractive candidate for medicinal chemistry research and drug development.
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