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51788-77-3

1-(2,4,6-Trifluorophenyl)ethanone

Catalog#: AR003GBY  |   CAS#: 51788-77-3  |   MDL#: MFCD00061194  |   MF: C8H5F3O  |   MW: 174.1199

Packsize Purity Price Availability Quantity
1g 98% $12.00 Global Stock Buy Now Add To Cart
5g 98% $36.00 Global Stock Buy Now Add To Cart
25g 98% $136.00 Global Stock Buy Now Add To Cart
100g 98% $456.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003GBY
Chemical Name 1-(2,4,6-Trifluorophenyl)ethanone
CAS Number 51788-77-3
Molecular Formula C8H5F3O
Molecular Weight 174.1199
MDL Number MFCD00061194
SMILES CC(=O)c1c(F)cc(cc1F)F

The compound 1-(2,4,6-Trifluorophenyl)ethanone, also known as $name$, is a versatile chemical reagent widely used in organic synthesis. Its unique structure, featuring a trifluorophenyl group attached to an ethanone moiety, imparts specific chemical properties that make it valuable for several synthetic applications.In chemical synthesis, $name$ serves as a key building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. It can participate in numerous transformations, such as nucleophilic additions, acylations, and reductions, due to the electrophilic nature of the ketone functional group. The trifluorophenyl group enhances the reactivity and stability of the molecule, allowing for efficient and selective reactions in complex synthetic pathways.Moreover, $name$ is commonly employed as a precursor for the synthesis of fluorinated compounds, which are of particular interest in medicinal chemistry and materials science. The trifluorophenyl substituent can facilitate fluorine incorporation into target molecules, leading to enhanced bioactivity, metabolic stability, and lipophilicity of the final products.Additionally, the presence of the trifluorophenyl group imparts unique physicochemical properties to compounds derived from $name$, making them suitable for diverse applications beyond traditional organic synthesis. These include use as molecular probes, fluorescent dyes, and building blocks in the development of advanced materials with tailored properties.Overall, the strategic incorporation of 1-(2,4,6-Trifluorophenyl)ethanone into synthetic pathways enables chemists to access a wide range of functionalized molecules with improved chemical and biological properties, driving innovation in drug discovery, materials science, and other fields of research.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H227-H315-H319
Precautionary Statements P210-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P403+P235-P501
Class N/A
Packing Group N/A

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