N-(Thiophen-2-ylmethyl)-3-(trifluoromethyl)benzenesulfonamide

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Reagent Code: #215831
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CAS Number 612042-35-0

science Other reagents with same CAS 612042-35-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.34 g/mol
Formula C₁₂H₁₀F₃NO₂S₂
thermostat Physical Properties
Boiling Point 418.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.436±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports binding to specific enzyme sites, making it valuable in developing anticonvulsant and neuroprotective agents. Also employed in agrochemical research for designing novel pesticides with improved stability and selectivity. The sulfonamide group enhances solubility and pharmacokinetic properties, while the trifluoromethyl and thiophene moieties contribute to metabolic resistance and target affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,320.00
inventory 250mg
10-20 days ฿19,990.00

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N-(Thiophen-2-ylmethyl)-3-(trifluoromethyl)benzenesulfonamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports binding to specific enzyme sites, making it valuable in developing anticonvulsant and neuroprotective agents. Also employed in agrochemical research for designing novel pesticides with improved stability and selectivity. The sulfonamide group enhances solubility and pharmacokinetic properties, while the trifluoromethyl and thiophene

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports binding to specific enzyme sites, making it valuable in developing anticonvulsant and neuroprotective agents. Also employed in agrochemical research for designing novel pesticides with improved stability and selectivity. The sulfonamide group enhances solubility and pharmacokinetic properties, while the trifluoromethyl and thiophene moieties contribute to metabolic resistance and target affinity.

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