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CAS 1087798-17-1

:

2,2,2-Trifluoroethyl N-(2,6-diethylphenyl)carbamate

Description:
2,2,2-Trifluoroethyl N-(2,6-diethylphenyl)carbamate is a chemical compound characterized by its unique structure, which includes a trifluoroethyl group and a carbamate functional group attached to a diethylphenyl moiety. This compound is typically a white to off-white solid at room temperature and is known for its stability under standard conditions. The presence of trifluoroethyl groups imparts notable properties, such as increased lipophilicity and potential bioactivity, making it of interest in various applications, including agrochemicals and pharmaceuticals. The carbamate functional group contributes to its reactivity, particularly in biological systems, where it may act as a substrate for enzymatic reactions. Additionally, the compound's molecular structure suggests potential interactions with biological targets, which can be explored for therapeutic purposes. Safety data and handling precautions should be considered, as with any chemical, to mitigate risks associated with exposure. Overall, 2,2,2-Trifluoroethyl N-(2,6-diethylphenyl)carbamate exemplifies the complexity and utility of fluorinated organic compounds in modern chemistry.
Formula:C13H16F3NO2
InChI:InChI=1S/C13H16F3NO2/c1-3-9-6-5-7-10(4-2)11(9)17-12(18)19-8-13(14,15)16/h5-7H,3-4,8H2,1-2H3,(H,17,18)
InChI key:InChIKey=VFGCFMJWJULUED-UHFFFAOYSA-N
SMILES:N(C(OCC(F)(F)F)=O)C1=C(CC)C=CC=C1CC
Synonyms:
  • 2,2,2-Trifluoroethyl N-(2,6-diethylphenyl)carbamate
  • 2,2,2-Trifluoroethyl 2,6-diethylphenylcarbamate
  • Carbamic acid, N-(2,6-diethylphenyl)-, 2,2,2-trifluoroethyl ester
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