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CAS 1087788-53-1

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2,2,2-Trifluoroethyl N-(2-methoxy-5-methylphenyl)carbamate

Description:
2,2,2-Trifluoroethyl N-(2-methoxy-5-methylphenyl)carbamate is a chemical compound characterized by its unique structure, which includes a trifluoroethyl group and a carbamate functional group. The presence of the trifluoroethyl moiety imparts notable properties such as increased lipophilicity and potential biological activity, making it of interest in various applications, including agrochemicals and pharmaceuticals. The carbamate group contributes to its reactivity and stability, while the aromatic ring with a methoxy and methyl substituent enhances its solubility and interaction with biological systems. This compound is typically synthesized through specific organic reactions involving carbamate formation and fluorinated alkylation. Its physical properties, such as boiling point, melting point, and solubility, are influenced by the trifluoromethyl group and the overall molecular structure. Additionally, the compound's safety and handling considerations are essential, as it may exhibit toxicity or environmental persistence, necessitating careful management in laboratory and industrial settings. Overall, 2,2,2-Trifluoroethyl N-(2-methoxy-5-methylphenyl)carbamate represents a significant compound in the realm of synthetic organic chemistry.
Formula:C11H12F3NO3
InChI:InChI=1S/C11H12F3NO3/c1-7-3-4-9(17-2)8(5-7)15-10(16)18-6-11(12,13)14/h3-5H,6H2,1-2H3,(H,15,16)
InChI key:InChIKey=PKKPVQOGJSJTEO-UHFFFAOYSA-N
SMILES:N(C(OCC(F)(F)F)=O)C1=C(OC)C=CC(C)=C1
Synonyms:
  • 2,2,2-Trifluoroethyl N-(2-methoxy-5-methylphenyl)carbamate
  • Carbamic acid, N-(2-methoxy-5-methylphenyl)-, 2,2,2-trifluoroethyl ester
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