Ethanone, 1-[2-fluoro-3-(trifluoromethyl)phenyl]-


Chemical Name: Ethanone, 1-[2-fluoro-3-(trifluoromethyl)phenyl]-
CAS Number: 207853-63-2
Product Number: AG002JC0(AGN-PC-0KK8KX)
Synonyms:
MDL No:
Molecular Formula: C9H6F4O
Molecular Weight: 206.1370

Identification/Properties


Properties
BP:
187.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
1.453
Computed Properties
Molecular Weight:
206.14g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
206.035g/mol
Monoisotopic Mass:
206.035g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
223
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



1-(2-Fluoro-3-(trifluoromethyl)phenyl)ethanone, also known as $name$, is a versatile compound that plays a crucial role in chemical synthesis. This compound is widely utilized as a key building block in the creation of complex organic molecules through various synthetic pathways.In chemical synthesis, $name$ serves as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural features and reactivity. It can be utilized as a precursor for the synthesis of biologically active compounds, enabling the modification of functional groups and enhancing desired properties.One of the primary applications of 1-(2-Fluoro-3-(trifluoromethyl)phenyl)ethanone in chemical synthesis is in the formation of heterocyclic compounds, which are vital in drug discovery and development. By incorporating $name$ into synthetic routes, chemists can access a wide range of diverse molecules with potential applications in medicinal chemistry and material science.Furthermore, this compound can participate in various transformations such as nucleophilic addition, condensation reactions, and cross-coupling processes, facilitating the creation of complex molecular architectures efficiently. Its strategic placement of fluorine and trifluoromethyl groups imparts desirable physicochemical properties to the synthesized compounds, enhancing their stability, lipophilicity, and bioactivity.Overall, 1-(2-Fluoro-3-(trifluoromethyl)phenyl)ethanone is a valuable tool in the hands of synthetic chemists, enabling the construction of diverse chemical structures with tailored functionalities for a wide range of applications in the field of organic chemistry.