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Home  > 2,2,2-Trifluoro-1-(3-fluoropyridin-2-yl)ethanone

AE28570

1060802-41-6 | 2,2,2-Trifluoro-1-(3-fluoropyridin-2-yl)ethanone

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $121.00 $85.00 -   +
250mg 95% in stock $169.00 $118.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE28570
Chemical Name: 2,2,2-Trifluoro-1-(3-fluoropyridin-2-yl)ethanone
CAS Number: 1060802-41-6
Molecular Formula: C7H3F4NO
Molecular Weight: 193.0984
MDL Number: MFCD13189065
SMILES: Fc1cccnc1C(=O)C(F)(F)F

 

Upstream Synthesis Route
  • The fluorinated compound 2,2,2-Trifluoro-1-(3-fluoropyridin-2-yl)ethanone, also known as $name$, is a valuable building block in chemical synthesis. This compound is widely utilized in organic chemistry as a versatile reagent for the introduction of trifluoromethyl and fluoroalkyl moieties into various organic molecules. Its unique structure enables it to participate in a range of reactions, including nucleophilic additions, substitution reactions, and metal-catalyzed transformations.In chemical synthesis, $name$ serves as a key intermediate for the preparation of pharmaceutically active compounds, agrochemicals, and materials with specialized properties. Its trifluoromethyl and fluoropyridine functionalities confer desirable properties such as increased metabolic stability, improved bioavailability, and enhanced binding affinity in drug molecules. Moreover, the presence of these fluorine atoms can influence the physicochemical properties of the final product, leading to compounds with enhanced lipophilicity, electron density, and interactions with biological targets.Researchers and industrial chemists leverage the reactivity of 2,2,2-Trifluoro-1-(3-fluoropyridin-2-yl)ethanone to synthesize complex molecules with tailored properties and functions. By strategically incorporating this compound into synthetic routes, chemists can access novel structural motifs and explore new chemical space for drug discovery, material science, and agrochemical development.
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