N-Methyl-N-[(trifluoromethyl)thio]-p-toluenesulfonamide

≥98%

Reagent Code: #217672
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CAS Number 1045822-31-8

science Other reagents with same CAS 1045822-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.3 g/mol
Formula C₉H₁₀F₃NO₂S₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly as a source of the trifluoromethylthio (SCF₃) group. This functional group is highly valued in medicinal chemistry and agrochemical research due to its strong electron-withdrawing properties and high lipophilicity, which can improve the metabolic stability and membrane permeability of bioactive molecules. The compound enables efficient trifluoromethylthiolation of various substrates, making it useful in the development of pharmaceuticals, pesticides, and specialty materials. Its stability and reactivity profile allow for selective transformations under mild conditions, which is advantageous in complex molecule synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,590.00
inventory 1g
10-20 days ฿10,200.00
inventory 5g
10-20 days ฿47,740.00
N-Methyl-N-[(trifluoromethyl)thio]-p-toluenesulfonamide
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Used as a key reagent in organic synthesis, particularly as a source of the trifluoromethylthio (SCF₃) group. This functional group is highly valued in medicinal chemistry and agrochemical research due to its strong electron-withdrawing properties and high lipophilicity, which can improve the metabolic stability and membrane permeability of bioactive molecules. The compound enables efficient trifluoromethylthiolation of various substrates, making it useful in the development of pharmaceuticals, pesticide

Used as a key reagent in organic synthesis, particularly as a source of the trifluoromethylthio (SCF₃) group. This functional group is highly valued in medicinal chemistry and agrochemical research due to its strong electron-withdrawing properties and high lipophilicity, which can improve the metabolic stability and membrane permeability of bioactive molecules. The compound enables efficient trifluoromethylthiolation of various substrates, making it useful in the development of pharmaceuticals, pesticides, and specialty materials. Its stability and reactivity profile allow for selective transformations under mild conditions, which is advantageous in complex molecule synthesis.

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