5-Methoxy-2-(trifluoromethyl)pyridine

≥97%

Reagent Code: #214359
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CAS Number 216766-13-1

science Other reagents with same CAS 216766-13-1

blur_circular Chemical Specifications

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Weight 177.12 g/mol
Formula C₇H₆F₃NO
badge Registry Numbers
MDL Number MFCD09864699
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and antidepressant drugs. Its structure supports metabolic stability and enhances binding affinity in central nervous system agents. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the electron-withdrawing trifluoromethyl and electron-donating methoxy groups that influence reactivity and selectivity. Also utilized in agrochemicals for developing herbicides and insecticides owing to its lipophilicity and resistance to degradation. Serves as a building block in cross-coupling reactions for creating complex pyridine-based compounds in research and industrial settings.

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inventory 10g
10-20 days ฿29,070.00

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5-Methoxy-2-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and antidepressant drugs. Its structure supports metabolic stability and enhances binding affinity in central nervous system agents. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the electron-withdrawing trifluoromethyl and electron-donating methoxy groups that influence reactivity and selectivity. Also utilized in agrochemicals for develo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and antidepressant drugs. Its structure supports metabolic stability and enhances binding affinity in central nervous system agents. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the electron-withdrawing trifluoromethyl and electron-donating methoxy groups that influence reactivity and selectivity. Also utilized in agrochemicals for developing herbicides and insecticides owing to its lipophilicity and resistance to degradation. Serves as a building block in cross-coupling reactions for creating complex pyridine-based compounds in research and industrial settings.

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