5-(Trifluoromethyl)picolinaldehyde

≥95%

Reagent Code: #241704
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CAS Number 31224-82-5

science Other reagents with same CAS 31224-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.11 g/mol
Formula C₇H₄F₃NO
badge Registry Numbers
MDL Number MFCD07375388
thermostat Physical Properties
Boiling Point 197.46°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its aldehyde group enables condensation reactions to form imines or other derivatives useful in drug discovery. Commonly employed in the preparation of kinase inhibitors and agrochemicals due to the electron-withdrawing trifluoromethyl group improving compound potency and lipophilicity. Also serves as a building block in materials science for designing functionalized ligands in catalysis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿960.00
inventory 1g
10-20 days ฿2,240.00
inventory 5g
10-20 days ฿10,400.00
inventory 25g
10-20 days ฿45,430.00

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5-(Trifluoromethyl)picolinaldehyde
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its aldehyde group enables condensation reactions to form imines or other derivatives useful in drug discovery. Commonly employed in the preparation of kinase inhibitors and agrochemicals due to the electron-withdrawing trifluoromethyl group improving compound potency and lipophilicity. Also serves as a building block in materials s

Used in the synthesis of pharmaceutical intermediates, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its aldehyde group enables condensation reactions to form imines or other derivatives useful in drug discovery. Commonly employed in the preparation of kinase inhibitors and agrochemicals due to the electron-withdrawing trifluoromethyl group improving compound potency and lipophilicity. Also serves as a building block in materials science for designing functionalized ligands in catalysis.

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