(2R,3R,4R,5R)-2-(Hydroxymethyl)-5-(2-isobutyramido-6-oxo-3,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate

95%

Reagent Code: #229375
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CAS Number 163586-86-5

science Other reagents with same CAS 163586-86-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 437.4 g/mol
Formula C₁₈H₂₃N₅O₈
inventory_2 Storage & Handling
Density 1.62±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of antiviral medications, particularly in the production of guanosine nucleoside analogs. These analogs are designed to mimic natural nucleosides, allowing them to interfere with viral replication processes. The compound's stereochemistry and functional groups make it suitable for incorporation into larger molecules that target DNA or RNA viruses. It is especially valuable in the development of drugs aimed at treating herpes infections, hepatitis B, HIV, and other viral infections. Its acetylated form helps improve stability during the synthetic process, facilitating easier handling and higher yields in pharmaceutical manufacturing.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,310.00
inventory 5g
10-20 days ฿8,080.00
inventory 25g
10-20 days ฿25,600.00

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(2R,3R,4R,5R)-2-(Hydroxymethyl)-5-(2-isobutyramido-6-oxo-3,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
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Used as an intermediate in the synthesis of antiviral medications, particularly in the production of guanosine nucleoside analogs. These analogs are designed to mimic natural nucleosides, allowing them to interfere with viral replication processes. The compound's stereochemistry and functional groups make it suitable for incorporation into larger molecules that target DNA or RNA viruses. It is especially valuable in the development of drugs aimed at treating herpes infections, hepatitis B, HIV, and other vi
Used as an intermediate in the synthesis of antiviral medications, particularly in the production of guanosine nucleoside analogs. These analogs are designed to mimic natural nucleosides, allowing them to interfere with viral replication processes. The compound's stereochemistry and functional groups make it suitable for incorporation into larger molecules that target DNA or RNA viruses. It is especially valuable in the development of drugs aimed at treating herpes infections, hepatitis B, HIV, and other viral infections. Its acetylated form helps improve stability during the synthetic process, facilitating easier handling and higher yields in pharmaceutical manufacturing.
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