S-(trifluoromethyl) 4-methoxybenzothioate

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Reagent Code: #236453
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CAS Number 1927969-11-6

science Other reagents with same CAS 1927969-11-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.215 g/mol
Formula C₉H₇F₃O₂S
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to introduce trifluoromethylthio groups into organic molecules. The presence of the electron-withdrawing trifluoromethyl group enhances metabolic stability and lipophilicity, improving the bioavailability and efficacy of active ingredients. Commonly employed in crop protection chemistry for designing compounds with improved environmental persistence and target specificity. Also utilized in medicinal chemistry research for exploring new bioactive molecules with potential antimicrobial or anti-inflammatory properties.

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inventory 1g
10-20 days ฿13,500.00

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S-(trifluoromethyl) 4-methoxybenzothioate
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to introduce trifluoromethylthio groups into organic molecules. The presence of the electron-withdrawing trifluoromethyl group enhances metabolic stability and lipophilicity, improving the bioavailability and efficacy of active ingredients. Commonly employed in crop protection chemistry for designing compounds with improved environmental persistenc

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to introduce trifluoromethylthio groups into organic molecules. The presence of the electron-withdrawing trifluoromethyl group enhances metabolic stability and lipophilicity, improving the bioavailability and efficacy of active ingredients. Commonly employed in crop protection chemistry for designing compounds with improved environmental persistence and target specificity. Also utilized in medicinal chemistry research for exploring new bioactive molecules with potential antimicrobial or anti-inflammatory properties.

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