S-(Trifluoromethyl) [1,1'-biphenyl]-4-carbothioate

98%

Reagent Code: #236790
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CAS Number 1927969-10-5

science Other reagents with same CAS 1927969-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.28 g/mol
Formula C₁₄H₉F₃OS
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to enhance metabolic stability and lipophilicity in active compounds. Its trifluoromethyl group contributes to improved bioavailability and resistance to oxidative degradation in biological systems. Commonly employed in cross-coupling reactions and sulfur-based functional group transformations in medicinal chemistry research. Also utilized in the design of advanced organic materials where electron-withdrawing properties are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,550.00
inventory 1g
10-20 days ฿6,800.00
inventory 5g
10-20 days ฿23,810.00
inventory 25g
10-20 days ฿83,270.00

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S-(Trifluoromethyl) [1,1'-biphenyl]-4-carbothioate
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to enhance metabolic stability and lipophilicity in active compounds. Its trifluoromethyl group contributes to improved bioavailability and resistance to oxidative degradation in biological systems. Commonly employed in cross-coupling reactions and sulfur-based functional group transformations in medicinal chemistry research. Also utilized in th

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to its ability to enhance metabolic stability and lipophilicity in active compounds. Its trifluoromethyl group contributes to improved bioavailability and resistance to oxidative degradation in biological systems. Commonly employed in cross-coupling reactions and sulfur-based functional group transformations in medicinal chemistry research. Also utilized in the design of advanced organic materials where electron-withdrawing properties are required.

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