CAS 59512-16-2
:2-[3-(phenylcarbonyl)phenyl]propanamide
Description:
2-[3-(Phenylcarbonyl)phenyl]propanamide, also known by its CAS number 59512-16-2, is an organic compound characterized by its amide functional group and a complex aromatic structure. This compound features a propanamide backbone, which is substituted with a phenylcarbonyl group at one end and a phenyl group at the other, contributing to its potential as a versatile building block in organic synthesis. The presence of the carbonyl group enhances its reactivity, making it suitable for various chemical reactions, including acylation and condensation. Its aromatic rings provide stability and can influence the compound's solubility and interaction with biological systems. Typically, such compounds exhibit moderate to high melting points and may be soluble in organic solvents. The compound's structural features suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. However, detailed studies on its biological activity and toxicity would be necessary to fully understand its potential uses and safety profile.
Formula:C16H15NO2
InChI:InChI=1/C16H15NO2/c1-11(16(17)19)13-8-5-9-14(10-13)15(18)12-6-3-2-4-7-12/h2-11H,1H3,(H2,17,19)
SMILES:CC(c1cccc(c1)C(=O)c1ccccc1)C(=N)O
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Found 5 products.
2-(3-Benzoylphenyl)propanamide
CAS:2-(3-Benzoylphenyl)propanamidePurity:95%Molecular weight:253.3g/molKetoprofen EP Impurity E
CAS:Formula:C16H15NO2Color and Shape:White To Off-White SolidMolecular weight:253.30(2RS)-2-(3-Benzoylphenyl)propanamide
CAS:Formula:C16H15NO2Color and Shape:NeatMolecular weight:253.30rac Ketoprofen Amide
CAS:Controlled Product<p>Applications An amide of Ketoprofen (K200800) with anti-inflammatory properties.<br>References Spickett, R.G.W. et al.: Eur. J. Med. Chem., 11, 7 (1976); Ueno, K., et al.: J. Med. Chem., 19, 941 (1976); Liversidge, G.G., Anal. Profiles Drug Subs., 10, 443 (1981);<br></p>Formula:C16H15NO2Color and Shape:WhiteMolecular weight:253.30





