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CAS 350-09-4

:

(2S)-3-phenyl-2-[(trifluoroacetyl)amino]propanoate

Description:
(2S)-3-phenyl-2-[(trifluoroacetyl)amino]propanoate, with the CAS number 350-09-4, is an organic compound characterized by its specific stereochemistry and functional groups. It features a chiral center at the second carbon, which is part of a propanoate structure, indicating that it is a derivative of propanoic acid. The presence of a phenyl group contributes to its aromatic characteristics, while the trifluoroacetylamino group introduces significant electronegativity due to the three fluorine atoms, enhancing its reactivity and potential applications in various chemical reactions. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its unique combination of functional groups allows for diverse interactions, making it a valuable compound in medicinal chemistry. Additionally, the trifluoroacetyl moiety can influence the compound's solubility and stability, which are critical factors in its practical applications. Overall, this compound exemplifies the complexity and utility of chiral organic molecules in chemical research and industry.
Formula:C11H9F3NO3
InChI:InChI=1/C11H10F3NO3/c12-11(13,14)10(18)15-8(9(16)17)6-7-4-2-1-3-5-7/h1-5,8H,6H2,(H,15,18)(H,16,17)/p-1/t8-/m0/s1
SMILES:c1ccc(cc1)C[C@@H](C(=O)[O-])N=C(C(F)(F)F)O
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