Methyl 2-(trifluoromethyl)nicotinate

98%

Reagent Code: #129385
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CAS Number 136483-17-5

science Other reagents with same CAS 136483-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.13 g/mol
Formula C₈H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD12828079
thermostat Physical Properties
Boiling Point 216.7±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.331±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of trifluoromethyl-substituted heterocycles, which are valuable for enhancing metabolic stability and lipophilicity in drug design. Commonly employed in medicinal chemistry for constructing nicotinate-based scaffolds with potential insecticidal, antifungal, or anti-inflammatory activity. Also utilized in research settings to develop novel fluorinated analogs with improved biological profiles.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,300.00
inventory 1g
10-20 days ฿8,590.00

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Methyl 2-(trifluoromethyl)nicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of trifluoromethyl-substituted heterocycles, which are valuable for enhancing metabolic stability and lipophilicity in drug design. Commonly employed in medicinal chemistry for constructing nicotinate-based scaffolds with potential insecticidal, antifungal, or anti-inflammatory activity. Also utilized in research settings to develop

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of trifluoromethyl-substituted heterocycles, which are valuable for enhancing metabolic stability and lipophilicity in drug design. Commonly employed in medicinal chemistry for constructing nicotinate-based scaffolds with potential insecticidal, antifungal, or anti-inflammatory activity. Also utilized in research settings to develop novel fluorinated analogs with improved biological profiles.

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