5-(Trifluoromethyl)thiophene-2-carboxylic acid

98%

Reagent Code: #240413
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CAS Number 128009-32-5

science Other reagents with same CAS 128009-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.15 g/mol
Formula C₆H₃F₃O₂S
badge Registry Numbers
MDL Number MFCD04421350
thermostat Physical Properties
Boiling Point 258.6±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.569±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the creation of compounds with enhanced metabolic stability and binding affinity due to the presence of fluorine atoms. Commonly employed in agrochemicals for designing herbicides and insecticides, where the trifluoromethyl group improves lipophilicity and environmental persistence. Also utilized in materials science for constructing functional organic materials with unique electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,860.00
inventory 1g
10-20 days ฿14,940.00
inventory 5g
10-20 days ฿64,920.00
5-(Trifluoromethyl)thiophene-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the creation of compounds with enhanced metabolic stability and binding affinity due to the presence of fluorine atoms. Commonly employed in agrochemicals for designing herbicides and insecticides, where the trifluoromethyl group improves lipophilicity and environmental persistence. Also utilized in materials science for constructing functional

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the creation of compounds with enhanced metabolic stability and binding affinity due to the presence of fluorine atoms. Commonly employed in agrochemicals for designing herbicides and insecticides, where the trifluoromethyl group improves lipophilicity and environmental persistence. Also utilized in materials science for constructing functional organic materials with unique electronic properties.

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