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CAS 110193-60-7

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Ethyl α-oxo-3-(trifluoromethyl)benzeneacetate

Description:
Ethyl α-oxo-3-(trifluoromethyl)benzeneacetate, with the CAS number 110193-60-7, is an organic compound characterized by its ester functional group and the presence of a trifluoromethyl group, which significantly influences its chemical properties. This compound typically appears as a colorless to pale yellow liquid and is known for its aromatic characteristics due to the benzene ring. The trifluoromethyl group enhances its lipophilicity and can affect its reactivity, making it useful in various synthetic applications. Ethyl α-oxo-3-(trifluoromethyl)benzeneacetate may exhibit moderate volatility and is soluble in organic solvents, which is common for esters. Its structure suggests potential applications in pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis. Additionally, the presence of the α-oxo group indicates that it may participate in various chemical reactions, such as condensation and acylation, making it a versatile compound in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C11H9F3O3
InChI:InChI=1S/C11H9F3O3/c1-2-17-10(16)9(15)7-4-3-5-8(6-7)11(12,13)14/h3-6H,2H2,1H3
InChI key:InChIKey=OYMTUYSGHGBXRS-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)(=O)C1=CC(C(F)(F)F)=CC=C1
Synonyms:
  • (3-Trifluoromethylphenyl)Glyoxylic Acid Ethyl Ester
  • 2-(3-Trifluoromethylphenyl)-2-oxoacetic acid ethyl ester
  • Benzeneacetic acid, α-oxo-3-(trifluoromethyl)-, ethyl ester
  • Ethyl (3-Trifluoromethylbenzoyl)Acetate
  • Ethyl (3-Trifluoromethylphenyl)Glyoxylate
  • Ethyl 2-Oxo-2-[3-(Trifluoromethyl)Phenyl]Acetate
  • Ethyl 3-(3-Trifluoromethyl-Phenyl)-3-Oxopropanoate
  • Ethyl Oxo[3-(Trifluoromethyl)Phenyl]Acetate
  • Ethyl α-oxo-3-(trifluoromethyl)benzeneacetate
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