4-(TRIFLUOROMETHOXY)BENZOTHIOAMIDE

98%

Reagent Code: #244892
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CAS Number 149169-34-6

science Other reagents with same CAS 149169-34-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.20 g/mol
Formula C₈H₆F₃NOS
badge Registry Numbers
MDL Number MFCD00068113
thermostat Physical Properties
Melting Point 124-126 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antifungal, antibacterial, and anticancer properties. Its structure supports the creation of thiazole and benzothiazole derivatives, which are common scaffolds in medicinal chemistry. Also employed in agrochemical research for designing novel pesticides and herbicides due to the stability and electron-withdrawing nature of the trifluoromethoxy group. The compound's reactivity allows for easy functionalization, making it valuable in building complex molecules in drug discovery and crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,630.00
inventory 100mg
10-20 days ฿1,460.00
inventory 1g
10-20 days ฿7,290.00

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4-(TRIFLUOROMETHOXY)BENZOTHIOAMIDE
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antifungal, antibacterial, and anticancer properties. Its structure supports the creation of thiazole and benzothiazole derivatives, which are common scaffolds in medicinal chemistry. Also employed in agrochemical research for designing novel pesticides and herbicides due to the stability and electron-withdrawing nature of the trifluoromethoxy group. The compound's reactivity al
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antifungal, antibacterial, and anticancer properties. Its structure supports the creation of thiazole and benzothiazole derivatives, which are common scaffolds in medicinal chemistry. Also employed in agrochemical research for designing novel pesticides and herbicides due to the stability and electron-withdrawing nature of the trifluoromethoxy group. The compound's reactivity allows for easy functionalization, making it valuable in building complex molecules in drug discovery and crop protection chemistry.
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