(2-Phenylpropan-2-yloxy)(trifluoromethyl)sulfane

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Reagent Code: #227317
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CAS Number 1640084-14-5

science Other reagents with same CAS 1640084-14-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.25 g/mol
Formula C₁₀H₁₁F₃OS
badge Registry Numbers
MDL Number MFCD30187371
thermostat Physical Properties
Boiling Point 187.9±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.225±0.06 g/cm3(Predicted)
Storage -20°C, dry, away from light

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in introducing trifluoromethylthio groups into organic molecules. The trifluoromethylthio moiety is highly valued in medicinal chemistry due to its strong electron-withdrawing properties and high lipophilicity, which can improve the metabolic stability and membrane permeability of drug candidates. It is particularly useful in the development of bioactive molecules where enhanced pharmacokinetic profiles are required. Additionally, it serves as a building block in the creation of novel sulfanyl-containing compounds for research in pesticide design and functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,790.00
inventory 1g
10-20 days ฿13,960.00
inventory 250mg
10-20 days ฿5,690.00

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(2-Phenylpropan-2-yloxy)(trifluoromethyl)sulfane
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in introducing trifluoromethylthio groups into organic molecules. The trifluoromethylthio moiety is highly valued in medicinal chemistry due to its strong electron-withdrawing properties and high lipophilicity, which can improve the metabolic stability and membrane permeability of drug candidates. It is particularly useful in the development of bioactive molecules where enhanced pharmac

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in introducing trifluoromethylthio groups into organic molecules. The trifluoromethylthio moiety is highly valued in medicinal chemistry due to its strong electron-withdrawing properties and high lipophilicity, which can improve the metabolic stability and membrane permeability of drug candidates. It is particularly useful in the development of bioactive molecules where enhanced pharmacokinetic profiles are required. Additionally, it serves as a building block in the creation of novel sulfanyl-containing compounds for research in pesticide design and functional materials.

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