Methyl 6-(trifluoromethyl) nicotinate

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Reagent Code: #205326
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CAS Number 221313-10-6

science Other reagents with same CAS 221313-10-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.13 g/mol
Formula C₈H₆F₃NO₂
thermostat Physical Properties
Melting Point 61-62°C
Boiling Point 209.4ºC at 760mmHg
inventory_2 Storage & Handling
Density 1.331g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and anti-inflammatory agents. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry for improving drug potency and bioavailability. Also employed in agrochemicals as a building block for herbicides and insecticides due to its electron-withdrawing properties and structural specificity. Commonly utilized in research settings for structure-activity relationship (SAR) studies involving heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿143.00
inventory 1g
10-20 days ฿330.00
inventory 25g
10-20 days ฿4,800.00
inventory 100g
10-20 days ฿18,990.00
inventory 5g
10-20 days ฿990.00
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Methyl 6-(trifluoromethyl) nicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and anti-inflammatory agents. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry for improving drug potency and bioavailability. Also employed in agrochemicals as a building block for herbicides and insecticides due to its electron-withdrawing properties and structural specificity. Commonly utilized in research se

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and anti-inflammatory agents. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry for improving drug potency and bioavailability. Also employed in agrochemicals as a building block for herbicides and insecticides due to its electron-withdrawing properties and structural specificity. Commonly utilized in research settings for structure-activity relationship (SAR) studies involving heterocyclic compounds.

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