3-((Trifluoromethyl)thio)benzaldehyde

95%

Reagent Code: #240664
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CAS Number 51748-27-7

science Other reagents with same CAS 51748-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.19 g/mol
Formula C₈H₅F₃OS
thermostat Physical Properties
Boiling Point 172.9°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its electrophilic aldehyde group allows for easy functionalization, enabling the formation of imines, oximes, or alcohols in multi-step reactions. The trifluoromethylthio group contributes high lipophilicity and electron-withdrawing properties, making this compound valuable in the design of biologically active molecules, including potential antifungal, antibacterial, and anti-inflammatory agents. It is also employed in the preparation of novel pesticides due to the favorable physicochemical properties imparted by the SCF3 moiety.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿1,880.00
inventory 5g
10-20 days ฿8,880.00
inventory 10g
10-20 days ฿17,660.00
inventory 25g
10-20 days ฿33,800.00
3-((Trifluoromethyl)thio)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its electrophilic aldehyde group allows for easy functionalization, enabling the formation of imines, oximes, or alcohols in multi-step reactions. The trifluoromethylthio group contributes high lipophilicity and electron-withdrawing properties, making this compound valuable in the design of biologically active mol

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its electrophilic aldehyde group allows for easy functionalization, enabling the formation of imines, oximes, or alcohols in multi-step reactions. The trifluoromethylthio group contributes high lipophilicity and electron-withdrawing properties, making this compound valuable in the design of biologically active molecules, including potential antifungal, antibacterial, and anti-inflammatory agents. It is also employed in the preparation of novel pesticides due to the favorable physicochemical properties imparted by the SCF3 moiety.

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