2,2,2-Trifluoro-1-(pyridin-3-yl)ethanone

95%

Reagent Code: #242534
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CAS Number 33284-21-8

science Other reagents with same CAS 33284-21-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.11 g/mol
Formula C₇H₄F₃NO
badge Registry Numbers
MDL Number MFCD00799596
thermostat Physical Properties
Boiling Point 197.9±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, inflatable

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and drugs targeting neurological disorders. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. Commonly employed in the preparation of trifluoromethyl-containing compounds, which often exhibit improved metabolic stability and binding affinity. Also utilized in agrochemical research for designing novel pesticides with higher efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,690.00
inventory 1g
10-20 days ฿17,450.00
inventory 100mg
10-20 days ฿5,200.00

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2,2,2-Trifluoro-1-(pyridin-3-yl)ethanone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and drugs targeting neurological disorders. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. Commonly employed in the preparation of trifluoromethyl-containing compounds, which often exhibit improved metabolic stability and binding affinity. Also utilized in agrochemical research for

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and drugs targeting neurological disorders. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. Commonly employed in the preparation of trifluoromethyl-containing compounds, which often exhibit improved metabolic stability and binding affinity. Also utilized in agrochemical research for designing novel pesticides with higher efficacy and selectivity.

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