(3R,3aS,6R,6aS)-hexahydrofuro[3,2-b]furan-3,6-diyl bis(4-methylbenzenesulfonate)

95%

Reagent Code: #230936
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CAS Number 67890-26-0

science Other reagents with same CAS 67890-26-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.51 g/mol
Formula C₂₀H₂₂O₈S₂
badge Registry Numbers
MDL Number MFCD25370320
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of complex natural products and pharmaceuticals, particularly in the preparation of HIV protease inhibitors such as Amprenavir and Darunavir. Its rigid bis-tetrahydrofuran bis-tosylate structure enables selective functionalization, ring-opening reactions, and stereoselective synthesis. Commonly employed in the development of antiviral protease inhibitors and carbohydrate mimetics due to its ability to mimic sugar moieties in enzyme active sites. Also utilized in polymer chemistry as a cross-linking agent for specialty resins.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,900.00
inventory 250mg
10-20 days ฿53,940.00
(3R,3aS,6R,6aS)-hexahydrofuro[3,2-b]furan-3,6-diyl bis(4-methylbenzenesulfonate)
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Used as a key intermediate in the synthesis of complex natural products and pharmaceuticals, particularly in the preparation of HIV protease inhibitors such as Amprenavir and Darunavir. Its rigid bis-tetrahydrofuran bis-tosylate structure enables selective functionalization, ring-opening reactions, and stereoselective synthesis. Commonly employed in the development of antiviral protease inhibitors and carbohydrate mimetics due to its ability to mimic sugar moieties in enzyme active sites. Also utilized i

Used as a key intermediate in the synthesis of complex natural products and pharmaceuticals, particularly in the preparation of HIV protease inhibitors such as Amprenavir and Darunavir. Its rigid bis-tetrahydrofuran bis-tosylate structure enables selective functionalization, ring-opening reactions, and stereoselective synthesis. Commonly employed in the development of antiviral protease inhibitors and carbohydrate mimetics due to its ability to mimic sugar moieties in enzyme active sites. Also utilized in polymer chemistry as a cross-linking agent for specialty resins.

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