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CAS 1087798-07-9

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2,2,2-Trifluoroethyl N-(3-fluoro-4-methylphenyl)carbamate

Description:
2,2,2-Trifluoroethyl N-(3-fluoro-4-methylphenyl)carbamate is a chemical compound characterized by its unique structure, which includes a trifluoroethyl group and a carbamate functional group. This compound is typically a white to off-white solid at room temperature and is known for its stability under standard conditions. It exhibits moderate solubility in organic solvents, which is common for carbamate derivatives. The presence of fluorine atoms in its structure contributes to its lipophilicity and potential biological activity, making it of interest in various fields, including agrochemicals and pharmaceuticals. The compound may also exhibit specific reactivity patterns due to the electron-withdrawing nature of the fluorine atoms, influencing its interactions with biological targets. Safety data should be consulted for handling and exposure guidelines, as fluorinated compounds can have unique toxicological profiles. Overall, 2,2,2-Trifluoroethyl N-(3-fluoro-4-methylphenyl)carbamate represents a class of compounds with potential applications in chemical synthesis and medicinal chemistry.
Formula:C10H9F4NO2
InChI:InChI=1S/C10H9F4NO2/c1-6-2-3-7(4-8(6)11)15-9(16)17-5-10(12,13)14/h2-4H,5H2,1H3,(H,15,16)
InChI key:InChIKey=VPRKTWJSRWMVCB-UHFFFAOYSA-N
SMILES:N(C(OCC(F)(F)F)=O)C1=CC(F)=C(C)C=C1
Synonyms:
  • 2,2,2-Trifluoroethyl N-(3-fluoro-4-methylphenyl)carbamate
  • Carbamic acid, N-(3-fluoro-4-methylphenyl)-, 2,2,2-trifluoroethyl ester
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