N-(Phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide

98%

Reagent Code: #220497
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CAS Number 1902154-93-1

science Other reagents with same CAS 1902154-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 397.41 g/mol
Formula C₁₃H₁₀F₃NO₄S₃
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a reagent in organic synthesis, particularly as a source of the trifluoromethylthio group (SCF₃). This compound enables the introduction of SCF₃ into target molecules, a functional group valued for its high lipophilicity and metabolic stability, making it especially useful in the development of pharmaceuticals and agrochemicals. It serves as a shelf-stable, easy-to-handle alternative to more volatile or toxic trifluoromethylthiolating agents. Commonly employed in radical and transition-metal-catalyzed reactions, it facilitates the late-stage functionalization of complex molecules, enhancing drug discovery efforts where fine-tuning of molecular properties is critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,880.00
inventory 250mg
10-20 days ฿3,760.00
inventory 1g
10-20 days ฿9,090.00
N-(Phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide
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Used as a reagent in organic synthesis, particularly as a source of the trifluoromethylthio group (SCF₃). This compound enables the introduction of SCF₃ into target molecules, a functional group valued for its high lipophilicity and metabolic stability, making it especially useful in the development of pharmaceuticals and agrochemicals. It serves as a shelf-stable, easy-to-handle alternative to more volatile or toxic trifluoromethylthiolating agents. Commonly employed in radical and transition-metal-cata

Used as a reagent in organic synthesis, particularly as a source of the trifluoromethylthio group (SCF₃). This compound enables the introduction of SCF₃ into target molecules, a functional group valued for its high lipophilicity and metabolic stability, making it especially useful in the development of pharmaceuticals and agrochemicals. It serves as a shelf-stable, easy-to-handle alternative to more volatile or toxic trifluoromethylthiolating agents. Commonly employed in radical and transition-metal-catalyzed reactions, it facilitates the late-stage functionalization of complex molecules, enhancing drug discovery efforts where fine-tuning of molecular properties is critical.

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