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CAS 53341-66-5

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ethyl 3-oxo-3-(phenylamino)propanoate

Description:
Ethyl 3-oxo-3-(phenylamino)propanoate, with the CAS number 53341-66-5, is an organic compound characterized by its ester functional group and a ketone moiety. It features a propanoate backbone with a phenylamino substituent, which contributes to its potential reactivity and biological activity. The presence of the phenylamino group suggests that this compound may exhibit properties associated with amines, such as basicity and the ability to participate in hydrogen bonding. The ester group indicates that it can undergo hydrolysis, transesterification, and other reactions typical of esters. This compound may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its structural features that could facilitate interactions with biological targets. Its solubility and stability in various solvents can vary, which is important for its application in different chemical processes. As with many organic compounds, safety and handling precautions should be observed, as it may pose health risks if not managed properly.
Formula:C11H13NO3
InChI:InChI=1/C11H13NO3/c1-2-15-11(14)8-10(13)12-9-6-4-3-5-7-9/h3-7H,2,8H2,1H3,(H,12,13)
SMILES:CCOC(=O)CC(=Nc1ccccc1)O
Synonyms:
  • Ethyl 3-anilino-3-oxopropanoate
  • Propanoic acid, 3-oxo-3-(phenylamino)-, ethyl ester
  • 2-Phenylcarbamoylacetic acid ethyl ester
  • ethyl 3-oxo-3-(phenylamino)propionate
  • 3-Ethoxy-3-oxo-N-phenylpropanamide
  • Ethyl 3-[N-(phenyl)amino]-3-oxopropionate
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