2-(Trifluoromethyl)nicotinaldehyde

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Reagent Code: #240672
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CAS Number 116308-35-1

science Other reagents with same CAS 116308-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.11 g/mol
Formula C₇H₄F₃NO
badge Registry Numbers
MDL Number MFCD08234912
thermostat Physical Properties
Boiling Point 207.9°C
inventory_2 Storage & Handling
Storage Room temperature, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in condensation reactions and cyclizations to build nitrogen-containing heterocycles. Also utilized in the preparation of fluorescent probes and functional materials due to its electron-withdrawing properties and reactivity profile.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿670.00
inventory 100mg
10-20 days ฿1,670.00
inventory 250mg
10-20 days ฿3,330.00
inventory 1g
10-20 days ฿10,410.00

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2-(Trifluoromethyl)nicotinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in condensation reactions and cyclizations to build nitrogen-containing heterocycles. Also utilized in the preparation of fluorescent probes and functional materials due to its electron-withdrawing propert

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in condensation reactions and cyclizations to build nitrogen-containing heterocycles. Also utilized in the preparation of fluorescent probes and functional materials due to its electron-withdrawing properties and reactivity profile.

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