CAS 94695-50-8
:Ethyl 2,3,4,5-tetrafluoro-β-oxobenzenepropanoate
Description:
Ethyl 2,3,4,5-tetrafluoro-β-oxobenzenepropanoate, with the CAS number 94695-50-8, is a fluorinated organic compound characterized by the presence of multiple fluorine atoms attached to a benzene ring, which significantly influences its chemical properties. The presence of the β-oxobenzene structure indicates that it contains a carbonyl group adjacent to the aromatic system, contributing to its reactivity and potential applications in organic synthesis. The ethyl ester functional group suggests that it can undergo hydrolysis to form the corresponding acid, making it versatile in various chemical reactions. The fluorine substituents enhance the compound's lipophilicity and thermal stability, which can be advantageous in pharmaceutical and agrochemical applications. Additionally, the unique combination of functional groups may impart specific biological activities, making it a subject of interest in medicinal chemistry. Overall, this compound exemplifies the importance of fluorinated derivatives in enhancing the properties of organic molecules for diverse applications.
Formula:C11H8F4O3
InChI:InChI=1/C11H8F4O3/c1-2-18-8(17)4-7(16)5-3-6(12)10(14)11(15)9(5)13/h3H,2,4H2,1H3
InChI key:InChIKey=KWDVJYLIAJHEOW-UHFFFAOYSA-N
SMILES:C(CC(OCC)=O)(=O)C1=C(F)C(F)=C(F)C(F)=C1
Synonyms:- 2,3,4,5-Tetrafluorobenzoyl acetic acid, ethyl ester
- 3-Oxo-3-(2,3,4,5-Tetrafluoro-Phenyl)-Propionic Acid Ethyl Ester
- 3-Oxo-3-(2,3,4,5-tetrafluorophenyl)propionic acid ethyl ester
- Benzenepropanoic acid, 2,3,4,5-tetrafluoro-β-oxo-, ethyl ester
- Ethyl 2,3,4,5-tetrafluoro-β-oxobenzenepropanoate
- Ethyl 2,3,4,5-tetrafluoro-β-oxobenzenepropionate
- Ethyl 2,3,4,5-tetrafluorobenzoylacetate
- Ethyl 2-(2,3,4,5-tetrafluorobenzoyl)acetate
- Ethyl 3-Oxo-3-(2,3,4,5-Tetrafluorophenyl)Propanoate
- Ethyl α-(2,3,4,5-tetrafluorobenzoyl)acetate
- Ethyl(2,3,4,5-tetrafluorobenzo
- Methyl (2,3,4,5-Tetrafluoro-Benzoyl)Acetate
- Ethyl 3-(2,3,4,5-tetrafluorophenyl)-3-oxopropanoate
- ETHYL 2,3,4,5-TETRAFLUOROBENZOYL ACETATE
- See more synonyms
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Found 7 products.
Ethyl (2,3,4,5-Tetrafluorobenzoyl)acetate
CAS:Formula:C11H8F4O3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:264.18Ethyl (2,3,4,5-Tetrafluorobenzoyl)acetate
CAS:Formula:C11H8F4O3Purity:97%Color and Shape:SolidMolecular weight:264.1730Ethyl 3-oxo-3-(2,3,4,5-tetrafluorophenyl)propanoate
CAS:Ethyl 3-oxo-3-(2,3,4,5-tetrafluorophenyl)propanoatePurity:≥95%Color and Shape:PowderMolecular weight:264.17303g/mol2,3,4,5-Tetrafluorobenzoylacetic Acid Ethyl Ester
CAS:Controlled Product<p>Applications 2,3,4,5-Tetrafluorobenzoylacetic Acid Ethyl Ester is a fluorinated benzoylacetate used as a synthetic reagent in the preparation of antibacterial and potential antitumor agents.<br>References Miyamoto, T. et al.: Chem. Pharmac. Bul., 36, 1321 (1988); Matsumoto, J. et al.: Qunilones, 109 (1989); Srivastava, S.K. et al.: Anti-Cancer Agents Med. Chem., 7, 685 (2007);<br></p>Formula:C11H8F4O3Color and Shape:NeatMolecular weight:264.17Ethyl (2,3,4,5-tetrafluorobenzoyl)acetate
CAS:<p>Ethyl (2,3,4,5-tetrafluorobenzoyl)acetate is a new oxazine derivative that inhibits bacterial growth by binding to the DNA gyrase and topoisomerase IV. It also exhibits antibacterial activity against Gram-positive bacteria such as methicillin-resistant Staphylococcus aureus (MRSA). This compound is an analog of the quinolone antibacterials. The most efficient example of this class of compounds is ofloxacin.</p>Formula:C11H8F4O3Purity:Min. 95%Color and Shape:PowderMolecular weight:264.17 g/molEthyl 3-oxo-3-(2,3,4,5-tetrafluorophenyl)propanoate
CAS:Ethyl 3-oxo-3-(2,3,4,5-tetrafluorophenyl)propanoate is a useful organic compound for research related to life sciences. The catalog number is T64869 and the CAS number is 94695-50-8.Formula:C11H8F4O3Color and Shape:SolidMolecular weight:264.176






