3-Methyl-5-(trifluoromethyl)picolinaldehyde

98%

Reagent Code: #130045
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CAS Number 780800-84-2

science Other reagents with same CAS 780800-84-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.14 g/mol
Formula C₈H₆F₃NO
badge Registry Numbers
MDL Number MFCD18261836
thermostat Physical Properties
Boiling Point 217.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.312±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its aldehyde functionality allows for easy derivatization, making it valuable in constructing complex molecules via condensation or reductive amination reactions. Commonly employed in the preparation of kinase inhibitors and other biologically active agents where the trifluoromethyl group contributes to improved lipophilicity and binding affinity. Also utilized in research settings for the design of novel heterocyclic systems with potential therapeutic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿27,550.00
inventory 100mg
10-20 days ฿12,520.00

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3-Methyl-5-(trifluoromethyl)picolinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its aldehyde functionality allows for easy derivatization, making it valuable in constructing complex molecules via condensation or reductive amination reactions. Commonly employed in the preparation of kinase inhibitors and other biologically active agents where the trifluoromethyl group contributes to improved l

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its aldehyde functionality allows for easy derivatization, making it valuable in constructing complex molecules via condensation or reductive amination reactions. Commonly employed in the preparation of kinase inhibitors and other biologically active agents where the trifluoromethyl group contributes to improved lipophilicity and binding affinity. Also utilized in research settings for the design of novel heterocyclic systems with potential therapeutic applications.

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