3-((Trifluoromethyl)thio)benzoic acid

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Reagent Code: #132079
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CAS Number 946-65-6

science Other reagents with same CAS 946-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.18 g/mol
Formula C₈H₅F₃O₂S
badge Registry Numbers
MDL Number MFCD00236337
thermostat Physical Properties
Melting Point 71-74 °C(lit.)
Boiling Point 229.5±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.50±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity due to the presence of the trifluoromethylthio group. It serves as a building block in medicinal chemistry for designing bioactive molecules, including potential antifungal, antibacterial, and anti-inflammatory agents. The compound's strong electron-withdrawing properties make it valuable in the preparation of fluorinated analogs in drug discovery programs. It is also employed in the creation of novel pesticides, where the trifluoromethylthio moiety contributes to improved pest control efficacy and environmental persistence.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,630.00
inventory 1g
10-20 days ฿4,790.00
inventory 5g
10-20 days ฿14,230.00

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3-((Trifluoromethyl)thio)benzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity due to the presence of the trifluoromethylthio group. It serves as a building block in medicinal chemistry for designing bioactive molecules, including potential antifungal, antibacterial, and anti-inflammatory agents. The compound's strong electron-withdrawing properties make it valuable in the preparation of fluorinated analogs i

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity due to the presence of the trifluoromethylthio group. It serves as a building block in medicinal chemistry for designing bioactive molecules, including potential antifungal, antibacterial, and anti-inflammatory agents. The compound's strong electron-withdrawing properties make it valuable in the preparation of fluorinated analogs in drug discovery programs. It is also employed in the creation of novel pesticides, where the trifluoromethylthio moiety contributes to improved pest control efficacy and environmental persistence.

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