76461-89-7

Basic information

• Product Name: N-(2-oxo-2H-chromen-3-yl)-3-phenylacrylamide
• CAS NO: 76461-89-7
• Molecular Weight: 291.306
• Mol File: 76461-89-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(2-oxo-2H-chromen-3-yl)-3-phenylacrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-oxo-2H-chromen-3-yl)-3-phenylacrylamide(76461-89-7)
• EPA Substance Registry System: N-(2-oxo-2H-chromen-3-yl)-3-phenylacrylamide(76461-89-7)

Safety Data

• Hazardous Substances Data: 76461-89-7(Hazardous Substances Data)

Upstream product

• 16534-24-0 (E)-cinnamoylglycine 
• 90-02-8 salicylaldehyde 
• 779-30-6 3-acetamidocoumarin 
• 2549-08-8 3-benzamidocoumarin 
• 115127-03-2 N-cinnamoylamino glycine 
• 1635-31-0 aminocoumarine 
• 140-10-3 (E)-3-phenylacrylic acid 
• 541-41-3 chloroformic acid ethyl ester 

Relevant articles and documents

Novel synthesis and cytotoxic activity of some chromeno[3,4-b]pyrrol-4(3H)- ones

1-Methylchromeno[3,4-b]pyrrol-4(3H)-one and 1-phenylchromeno[3,4-b]pyrrol- 4(3H)-one derivatives have been synthesized by cyclization of amides obtained by condensing α-halo ketones with 3-amino-chromenones, which show cytotoxic activity against lung, colon, and breast cancer cell lines.

Reactions of 2-Substituted 5-Oxazolones with Imines Carrying a Vicinal Hydroxyl Group & Salicylaldehyde

5-Oxazolones, generated by cyclising N-acylglycines with ethyl chloroformate, react with imines carrying a vicinal hydroxyl group and also with salicylaldehyde.Unsaturated 5-oxazolone or 3-N-acylaminocoumarin is obtained depending on the type of reactants.