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CAS 1208081-82-6

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N-[6-Chloro-4-(trifluoromethyl)-2-pyridinyl]glycine ethyl ester

Description:
N-[6-Chloro-4-(trifluoromethyl)-2-pyridinyl]glycine ethyl ester is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with a chlorine atom and a trifluoromethyl group. This compound is typically classified as an amino acid derivative due to the presence of the glycine moiety. The ethyl ester functional group enhances its lipophilicity, potentially influencing its biological activity and solubility in organic solvents. The presence of the trifluoromethyl group is notable for imparting unique electronic properties, which can affect the compound's reactivity and interactions with biological targets. This compound may be of interest in pharmaceutical research, particularly in the development of new therapeutic agents, due to its potential biological activity linked to the pyridine structure. Additionally, the chlorine and trifluoromethyl substituents can enhance the compound's pharmacokinetic properties, making it a candidate for further investigation in medicinal chemistry. As with many chemical substances, safety and handling precautions should be observed, given the presence of halogenated groups.
Formula:C10H10ClF3N2O2
InChI:InChI=1S/C10H10ClF3N2O2/c1-2-18-9(17)5-15-8-4-6(10(12,13)14)3-7(11)16-8/h3-4H,2,5H2,1H3,(H,15,16)
InChI key:InChIKey=SOWHJBNHOLUGTL-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C=C(NCC(OCC)=O)N=C(Cl)C1
Synonyms:
  • N-[6-Chloro-4-(trifluoromethyl)-2-pyridinyl]glycine ethyl ester
  • Glycine, N-[6-chloro-4-(trifluoromethyl)-2-pyridinyl]-, ethyl ester
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