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CAS 115957-22-7

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3-(2-THIENYL)-3-[(2,2,2-TRIFLUOROACETYL)AMINO]PROPANOIC ACID

Description:
3-(2-Thienyl)-3-[(2,2,2-trifluoroacetyl)amino]propanoic acid is an organic compound characterized by its unique structural features, which include a thienyl group and a trifluoroacetylamino moiety. The presence of the thienyl ring contributes to its aromatic properties, while the trifluoroacetyl group enhances its reactivity and solubility in polar solvents. This compound is likely to exhibit acidic behavior due to the carboxylic acid functional group, which can donate protons in solution. The trifluoromethyl group is known for its electron-withdrawing effects, which can influence the compound's overall reactivity and stability. Additionally, the presence of fluorine atoms can impart unique physical properties, such as increased lipophilicity and altered boiling and melting points compared to non-fluorinated analogs. Overall, this compound may have applications in medicinal chemistry and material science, particularly in the development of pharmaceuticals or agrochemicals, owing to its distinctive chemical characteristics.
Formula:C9H7F3NO3S
InChI:InChI=1/C9H8F3NO3S/c10-9(11,12)8(16)13-5(4-7(14)15)6-2-1-3-17-6/h1-3,5H,4H2,(H,13,16)(H,14,15)/p-1/t5-/m1/s1
SMILES:c1cc([C@@H](CC(=O)[O-])N=C(C(F)(F)F)O)sc1
Synonyms:
  • 3-(Thien-2-yl)-3-[(2,2,2-trifluoroacetyl)amino]propanoic acid
  • 3-Thiophen-2-Yl-3-[(Trifluoroacetyl)Amino]Propanoic Acid
  • (3S)-3-thiophen-2-yl-3-[(trifluoroacetyl)amino]propanoate
  • (3R)-3-thiophen-2-yl-3-[(trifluoroacetyl)amino]propanoate
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