Methyl 3-(trifluoromethyl)pyridine-2-carboxylate

≥95%

Reagent Code: #205646
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CAS Number 588702-69-6

science Other reagents with same CAS 588702-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.13 g/mol
Formula C₈H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD14698094
thermostat Physical Properties
Boiling Point 256.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.331±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the construction of complex heterocyclic compounds, making it valuable in medicinal chemistry for creating analogs with potential antifungal, antibacterial, or anti-inflammatory properties. Commonly employed in research settings for derivatization and scaffold modification in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿850.00
inventory 5g
10-20 days ฿3,830.00
inventory 10g
10-20 days ฿7,620.00
inventory 25g
10-20 days ฿16,550.00
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Methyl 3-(trifluoromethyl)pyridine-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the construction of complex heterocyclic compounds, making it valuable in medicinal chemistry for creating analogs with potential antifungal, antibacterial, or anti-inflammatory properties. Commonly employed in research settings for derivatization and scaffold modification in drug discovery programs.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the construction of complex heterocyclic compounds, making it valuable in medicinal chemistry for creating analogs with potential antifungal, antibacterial, or anti-inflammatory properties. Commonly employed in research settings for derivatization and scaffold modification in drug discovery programs.

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