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CAS 196202-01-4

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Methyl 2,2-difluoro-3-oxopentanoate

Description:
Methyl 2,2-difluoro-3-oxopentanoate is an organic compound characterized by its ester functional group, which is typical of carboxylic acid derivatives. It features a pentanoate backbone with a ketone functional group at the third carbon and two fluorine atoms attached to the second carbon, contributing to its unique reactivity and properties. The presence of fluorine atoms often enhances the compound's lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry and agrochemicals. The methyl ester group indicates that it is a methyl ester, which typically exhibits good solubility in organic solvents. This compound may also participate in various chemical reactions, such as nucleophilic substitutions or condensation reactions, due to the electrophilic nature of the carbonyl group. Its specific applications can vary, but it may be utilized in the synthesis of more complex molecules or as an intermediate in organic synthesis. Safety and handling precautions should be observed, as with many fluorinated compounds, due to potential toxicity and environmental concerns.
Formula:C11H12F6O
InChI:InChI=1/C11H12F6O/c12-10(13,14)9(18,11(15,16)17)5-8-4-6-1-2-7(8)3-6/h1-2,6-8,18H,3-5H2
SMILES:C1=CC2CC1CC2CC(C(F)(F)F)(C(F)(F)F)O
Synonyms:
  • 2-(Bicyclo[2.2.1]Hept-5-En-2-Ylmethyl)-1,1,1,3,3,3-Hexafluoropropan-2-Ol
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