2-(Trifluoromethoxy)thiophenol

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Reagent Code: #244847
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CAS Number 175278-01-0

science Other reagents with same CAS 175278-01-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.18 g/mol
Formula C₇H₅F₃OS
badge Registry Numbers
MDL Number MFCD00052320
thermostat Physical Properties
Boiling Point 53-55 °C
inventory_2 Storage & Handling
Density 1.363±0.06 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 fluorinated organic compounds. Its trifluoromethoxy and thiol functional groups enable selective reactions in building complex molecules, especially in medicinal chemistry for enhancing metabolic stability and lipophilicity. Also employed in the preparation of specialty polymers and ligands for catalysis due to the strong electron-withdrawing nature of the trifluoromethoxy group and the coordinating ability of the thiol.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿54,830.00

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2-(Trifluoromethoxy)thiophenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its trifluoromethoxy and thiol functional groups enable selective reactions in building complex molecules, especially in medicinal chemistry for enhancing metabolic stability and lipophilicity. Also employed in the preparation of specialty polymers and ligands for catalysis due to the strong electron-withdrawing nature of the trifluoromethoxy group and the coord

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its trifluoromethoxy and thiol functional groups enable selective reactions in building complex molecules, especially in medicinal chemistry for enhancing metabolic stability and lipophilicity. Also employed in the preparation of specialty polymers and ligands for catalysis due to the strong electron-withdrawing nature of the trifluoromethoxy group and the coordinating ability of the thiol.

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