CAS 898766-13-7
:2,3-Difluoro-δ-oxobenzenepentanoic acid
Description:
2,3-Difluoro-δ-oxobenzenepentanoic acid is a chemical compound characterized by its unique structure, which includes a pentanoic acid backbone and a benzene ring with two fluorine substituents at the 2 and 3 positions. This compound features a keto group (oxobenzene) that contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of fluorine atoms typically enhances the lipophilicity and metabolic stability of the compound, which can be advantageous in drug design. The molecular structure suggests that it may exhibit interesting biological activities, although specific biological data would depend on empirical studies. Additionally, the compound's properties, such as solubility, melting point, and reactivity, would be influenced by the functional groups present and their spatial arrangement. As with many fluorinated compounds, it may also exhibit unique interactions with biological systems, making it a subject of interest in various fields, including pharmaceuticals and agrochemicals.
Formula:C11H10F2O3
InChI:InChI=1S/C11H10F2O3/c12-8-4-1-3-7(11(8)13)9(14)5-2-6-10(15)16/h1,3-4H,2,5-6H2,(H,15,16)
InChI key:InChIKey=UXSXZFMQBCGRRQ-UHFFFAOYSA-N
SMILES:C(CCCC(O)=O)(=O)C1=C(F)C(F)=CC=C1
Synonyms:- 2,3-Difluoro-δ-oxobenzenepentanoic acid
- Benzenepentanoic acid, 2,3-difluoro-δ-oxo-
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