(3aR,5R,6aS)-5-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyldihydrofuro[2,3-d][1,3]dioxol-6(3aH)-one

≥95%

Reagent Code: #232241
fingerprint
CAS Number 2847-00-9

science Other reagents with same CAS 2847-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.27 g/mol
Formula C₁₂H₁₈O₆
badge Registry Numbers
MDL Number MFCD00040456
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in the synthesis of antiviral drugs, particularly as an intermediate in the production of nucleoside analogs. It serves as a chiral building block in the development of pharmaceuticals targeting RNA viruses, including hepatitis C and SARS-CoV-2. Its rigid, polycyclic structure with multiple oxygen-containing rings helps mimic sugar moieties in nucleosides, enhancing binding selectivity to viral polymerases. Commonly employed in stereoselective synthesis to maintain desired configuration in active pharmaceutical ingredients.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3aR,5R,6aS)-5-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyldihydrofuro[2,3-d][1,3]dioxol-6(3aH)-one
No image available

Used in the synthesis of antiviral drugs, particularly as an intermediate in the production of nucleoside analogs. It serves as a chiral building block in the development of pharmaceuticals targeting RNA viruses, including hepatitis C and SARS-CoV-2. Its rigid, polycyclic structure with multiple oxygen-containing rings helps mimic sugar moieties in nucleosides, enhancing binding selectivity to viral polymerases. Commonly employed in stereoselective synthesis to maintain desired configuration in active ph

Used in the synthesis of antiviral drugs, particularly as an intermediate in the production of nucleoside analogs. It serves as a chiral building block in the development of pharmaceuticals targeting RNA viruses, including hepatitis C and SARS-CoV-2. Its rigid, polycyclic structure with multiple oxygen-containing rings helps mimic sugar moieties in nucleosides, enhancing binding selectivity to viral polymerases. Commonly employed in stereoselective synthesis to maintain desired configuration in active pharmaceutical ingredients.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...