(2R,3R,4R,5R)-2-(Hydroxymethyl)-5-[2-isobutyramido-6-oxo-1H-purin-9(6H)-yl]tetrahydrofuran-3,4-diyl Bis(2-methylpropanoate)

97%

Reagent Code: #229129
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CAS Number 56489-75-9

science Other reagents with same CAS 56489-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 493.51 g/mol
Formula C₂₂H₃₁N₅O₈
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of antiviral medications, particularly in the production of nucleoside analogs. These analogs are designed to mimic natural nucleosides, allowing them to interfere with viral replication processes. The compound's protected sugar moiety and modified base make it suitable for controlled coupling reactions in multi-step drug synthesis. It is especially valuable in the development of therapeutics targeting RNA viruses, where precise stereochemistry is critical for biological activity. Its ester-protected form enhances stability and solubility during synthesis, facilitating purification and handling in non-aqueous environments.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,200.00
inventory 500mg
10-20 days ฿45,600.00
inventory 1g
10-20 days ฿60,800.00
inventory 250mg
10-20 days ฿30,400.00

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(2R,3R,4R,5R)-2-(Hydroxymethyl)-5-[2-isobutyramido-6-oxo-1H-purin-9(6H)-yl]tetrahydrofuran-3,4-diyl Bis(2-methylpropanoate)
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Used as an intermediate in the synthesis of antiviral medications, particularly in the production of nucleoside analogs. These analogs are designed to mimic natural nucleosides, allowing them to interfere with viral replication processes. The compound's protected sugar moiety and modified base make it suitable for controlled coupling reactions in multi-step drug synthesis. It is especially valuable in the development of therapeutics targeting RNA viruses, where precise stereochemistry is critical for bio

Used as an intermediate in the synthesis of antiviral medications, particularly in the production of nucleoside analogs. These analogs are designed to mimic natural nucleosides, allowing them to interfere with viral replication processes. The compound's protected sugar moiety and modified base make it suitable for controlled coupling reactions in multi-step drug synthesis. It is especially valuable in the development of therapeutics targeting RNA viruses, where precise stereochemistry is critical for biological activity. Its ester-protected form enhances stability and solubility during synthesis, facilitating purification and handling in non-aqueous environments.

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