((2R,3R,4R)-3-(benzoyloxy)-4-fluoro-4-methyl-5-oxotetrahydrofuran-2-yl)methyl benzoate

98%

Reagent Code: #229974
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CAS Number 874638-80-9

science Other reagents with same CAS 874638-80-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.34 g/mol
Formula C₂₀H₁₇FO₆
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of antiviral medications, particularly in the production of nucleoside analogs. Its fluorinated tetrahydrofuran core enables enhanced metabolic stability and bioavailability in final drug compounds. Commonly employed in the development of experimental therapies targeting RNA viruses, where the benzoate ester groups assist in membrane permeability. Also utilized in stereoselective synthesis due to its defined chiral centers, allowing precise construction of complex pharmaceutical molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿350.00
25g
10-20 days ฿790.00
100g
10-20 days ฿3,020.00
500g
10-20 days ฿11,950.00
((2R,3R,4R)-3-(benzoyloxy)-4-fluoro-4-methyl-5-oxotetrahydrofuran-2-yl)methyl benzoate
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Used as a key intermediate in the synthesis of antiviral medications, particularly in the production of nucleoside analogs. Its fluorinated tetrahydrofuran core enables enhanced metabolic stability and bioavailability in final drug compounds. Commonly employed in the development of experimental therapies targeting RNA viruses, where the benzoate ester groups assist in membrane permeability. Also utilized in stereoselective synthesis due to its defined chiral centers, allowing precise construction of complex
Used as a key intermediate in the synthesis of antiviral medications, particularly in the production of nucleoside analogs. Its fluorinated tetrahydrofuran core enables enhanced metabolic stability and bioavailability in final drug compounds. Commonly employed in the development of experimental therapies targeting RNA viruses, where the benzoate ester groups assist in membrane permeability. Also utilized in stereoselective synthesis due to its defined chiral centers, allowing precise construction of complex pharmaceutical molecules.
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