6-(trifluoromethyl)pyridine-2-carbaldehyde

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Reagent Code: #240190
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CAS Number 131747-65-4

science Other reagents with same CAS 131747-65-4

blur_circular Chemical Specifications

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Weight 175.11 g/mol
Formula C₇H₄F₃NO
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MDL Number MFCD10696233
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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 aldehyde group allows for easy functionalization, enabling the formation of imines, oximes, and other derivatives important in medicinal chemistry. Frequently employed in the preparation of pyridine-based ligands and catalysts due to the electron-withdrawing effect of the trifluoromethyl group, which enhances stability and influences reactivity. Also utilized in the creation of fluorescent probes and sensors, where the trifluoromethylpyridine scaffold contributes to improved lipophilicity and membrane permeability in biological systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,600.00
inventory 250mg
10-20 days ฿2,580.00
inventory 1g
10-20 days ฿5,670.00
inventory 5g
10-20 days ฿23,280.00

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6-(trifluoromethyl)pyridine-2-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its aldehyde group allows for easy functionalization, enabling the formation of imines, oximes, and other derivatives important in medicinal chemistry. Frequently employed in the preparation of pyridine-based ligands and catalysts due to the electron-withdrawing effect of the trifluoromethyl group, which enhances stability and influences reactivity. Also utilized in th

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its aldehyde group allows for easy functionalization, enabling the formation of imines, oximes, and other derivatives important in medicinal chemistry. Frequently employed in the preparation of pyridine-based ligands and catalysts due to the electron-withdrawing effect of the trifluoromethyl group, which enhances stability and influences reactivity. Also utilized in the creation of fluorescent probes and sensors, where the trifluoromethylpyridine scaffold contributes to improved lipophilicity and membrane permeability in biological systems.

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