S-(Trifluoromethyl) benzenesulfonothioate

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Reagent Code: #236567
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CAS Number 15398-96-6

science Other reagents with same CAS 15398-96-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.24 g/mol
Formula C₇H₅F₃O₂S₂
inventory_2 Storage & Handling
Storage -20°C, dry, away from light

description Product Description

Used as a trifluoromethylthiolating agent in organic synthesis, enabling the introduction of the trifluoromethylthio (SCF3) group into various organic molecules. This transformation is valuable in pharmaceutical and agrochemical industries, where the SCF3 group can enhance metabolic stability, lipophilicity, and bioavailability of active compounds. It participates in radical and transition-metal-catalyzed reactions, offering a versatile method for C–SCF3 bond formation. Its reactivity allows for selective functionalization under mild conditions, making it suitable for complex molecule synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,690.00
inventory 250mg
10-20 days ฿4,560.00
inventory 1g
10-20 days ฿12,300.00
inventory 5g
10-20 days ฿45,880.00
S-(Trifluoromethyl) benzenesulfonothioate
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Used as a trifluoromethylthiolating agent in organic synthesis, enabling the introduction of the trifluoromethylthio (SCF3) group into various organic molecules. This transformation is valuable in pharmaceutical and agrochemical industries, where the SCF3 group can enhance metabolic stability, lipophilicity, and bioavailability of active compounds. It participates in radical and transition-metal-catalyzed reactions, offering a versatile method for C–SCF3 bond formation. Its
Used as a trifluoromethylthiolating agent in organic synthesis, enabling the introduction of the trifluoromethylthio (SCF3) group into various organic molecules. This transformation is valuable in pharmaceutical and agrochemical industries, where the SCF3 group can enhance metabolic stability, lipophilicity, and bioavailability of active compounds. It participates in radical and transition-metal-catalyzed reactions, offering a versatile method for C–SCF3 bond formation. Its reactivity allows for selective functionalization under mild conditions, making it suitable for complex molecule synthesis.
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