4-Hydroxy-2-(trifluoromethyl)thiophene

98%

Reagent Code: #196667
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CAS Number 217959-45-0

science Other reagents with same CAS 217959-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.14 g/mol
Formula C₅H₃F₃OS
badge Registry Numbers
MDL Number MFCD07779810
thermostat Physical Properties
Boiling Point 145.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential antifungal, antibacterial, or anti-inflammatory properties. Its structure supports derivatization for use in medicinal chemistry, especially in creating fluorinated heterocyclic compounds known for enhanced metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing trifluoromethyl group improving compound efficacy.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,550.00
250mg
10-20 days ฿11,030.00
4-Hydroxy-2-(trifluoromethyl)thiophene
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential antifungal, antibacterial, or anti-inflammatory properties. Its structure supports derivatization for use in medicinal chemistry, especially in creating fluorinated heterocyclic compounds known for enhanced metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing trifluoromethyl
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential antifungal, antibacterial, or anti-inflammatory properties. Its structure supports derivatization for use in medicinal chemistry, especially in creating fluorinated heterocyclic compounds known for enhanced metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing trifluoromethyl group improving compound efficacy.
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