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CAS 1415564-98-5

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4-Fluoro-3-nitrophenyl 2,2-dimethylpropanoate

Description:
4-Fluoro-3-nitrophenyl 2,2-dimethylpropanoate is an organic compound characterized by its functional groups and structural features. It contains a phenyl ring substituted with both a fluoro group and a nitro group, which contribute to its reactivity and potential applications in various chemical reactions. The ester functional group, derived from 2,2-dimethylpropanoic acid, indicates that this compound can participate in esterification and hydrolysis reactions. The presence of the fluoro and nitro substituents can enhance the compound's electrophilicity, making it useful in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the steric hindrance introduced by the dimethyl groups may influence its solubility and reactivity. Overall, this compound's unique combination of functional groups and structural characteristics makes it a subject of interest for further research and application in chemical synthesis.
Formula:C11H12FNO4
InChI:InChI=1S/C11H12FNO4/c1-11(2,3)10(14)17-7-4-5-8(12)9(6-7)13(15)16/h4-6H,1-3H3
InChI key:InChIKey=JZHPBVPEPYHRLD-UHFFFAOYSA-N
SMILES:O(C(C(C)(C)C)=O)C1=CC(N(=O)=O)=C(F)C=C1
Synonyms:
  • Propanoic acid, 2,2-dimethyl-, 4-fluoro-3-nitrophenyl ester
  • 4-Fluoro-3-nitrophenyl 2,2-dimethylpropanoate
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