S-(trifluoromethyl) 2-methoxybenzothioate

97%

Reagent Code: #236454
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CAS Number 1927969-13-8

science Other reagents with same CAS 1927969-13-8

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 a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing the biological activity of active ingredients. Commonly employed in sulfur-based coupling reactions to introduce functionalized benzothioate moieties into target molecules. Also utilized in research for designing novel compounds with improved environmental persistence and target specificity in crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,700.00
S-(trifluoromethyl) 2-methoxybenzothioate
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing the biological activity of active ingredients. Commonly employed in sulfur-based coupling reactions to introduce functionalized benzothioate moieties into target molecules. Also utilized in research for designing novel compounds with improved environmental p

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing the biological activity of active ingredients. Commonly employed in sulfur-based coupling reactions to introduce functionalized benzothioate moieties into target molecules. Also utilized in research for designing novel compounds with improved environmental persistence and target specificity in crop protection chemistry.

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