S-(trifluoromethyl) 4-chlorobenzenesulfonothioate

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Reagent Code: #236451
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CAS Number 17041-78-0

science Other reagents with same CAS 17041-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.687 g/mol
Formula C₇H₄ClF₃O₂S₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as a specialized reagent in organic synthesis, particularly in the introduction of trifluoromethylthio groups into bioactive molecules. Its high electrophilicity makes it effective for trifluoromethylthiolation of aromatic and heteroaromatic compounds, which is valuable in the development of pharmaceuticals and agrochemicals. The presence of the 4-chlorobenzenesulfonyl group enhances stability and selectivity during reactions. Commonly applied in medicinal chemistry for modifying lead compounds to improve metabolic stability and lipophilicity, aiding in the optimization of drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿15,470.00
S-(trifluoromethyl) 4-chlorobenzenesulfonothioate
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Used as a specialized reagent in organic synthesis, particularly in the introduction of trifluoromethylthio groups into bioactive molecules. Its high electrophilicity makes it effective for trifluoromethylthiolation of aromatic and heteroaromatic compounds, which is valuable in the development of pharmaceuticals and agrochemicals. The presence of the 4-chlorobenzenesulfonyl group enhances stability and selectivity during reactions. Commonly applied in medicinal chemistry for modifying lead compounds to i

Used as a specialized reagent in organic synthesis, particularly in the introduction of trifluoromethylthio groups into bioactive molecules. Its high electrophilicity makes it effective for trifluoromethylthiolation of aromatic and heteroaromatic compounds, which is valuable in the development of pharmaceuticals and agrochemicals. The presence of the 4-chlorobenzenesulfonyl group enhances stability and selectivity during reactions. Commonly applied in medicinal chemistry for modifying lead compounds to improve metabolic stability and lipophilicity, aiding in the optimization of drug candidates.

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