(R)-1-((3aR,5R,6S,6aR)-6-(Benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)-2-((tert-butyldimethylsilyl)oxy)ethan-1-ol

95%

Reagent Code: #228582
fingerprint
CAS Number 106445-04-9

science Other reagents with same CAS 106445-04-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 424.6 g/mol
Formula C₂₂H₃₆O₆Si
thermostat Physical Properties
Boiling Point 469.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of antiviral agents, particularly in the production of nucleoside analogs like Remdesivir. Its protected hydroxyl and diol functionalities allow selective reactions during multi-step synthesis, ensuring correct stereochemistry. The compound enables efficient construction of the ribose-like sugar moiety critical for biological activity. Commonly employed in pharmaceutical research and development for antiviral drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,810.00
inventory 1g
10-20 days ฿90,750.00
(R)-1-((3aR,5R,6S,6aR)-6-(Benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)-2-((tert-butyldimethylsilyl)oxy)ethan-1-ol
No image available

Used as a key chiral intermediate in the synthesis of antiviral agents, particularly in the production of nucleoside analogs like Remdesivir. Its protected hydroxyl and diol functionalities allow selective reactions during multi-step synthesis, ensuring correct stereochemistry. The compound enables efficient construction of the ribose-like sugar moiety critical for biological activity. Commonly employed in pharmaceutical research and development for antiviral drug candidates.

Used as a key chiral intermediate in the synthesis of antiviral agents, particularly in the production of nucleoside analogs like Remdesivir. Its protected hydroxyl and diol functionalities allow selective reactions during multi-step synthesis, ensuring correct stereochemistry. The compound enables efficient construction of the ribose-like sugar moiety critical for biological activity. Commonly employed in pharmaceutical research and development for antiviral drug candidates.

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

Purchase History for

Loading purchase history...