213273-03-1

Basic information

• Product Name: 4H-1-Benzopyran-3-carboxaldehyde, 4-oxo-2-(phenylamino)-
• CAS NO: 213273-03-1
• Molecular Formula: C16H11NO3
• Molecular Weight: 265.268
• Mol File: 213273-03-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 4H-1-Benzopyran-3-carboxaldehyde, 4-oxo-2-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1-Benzopyran-3-carboxaldehyde, 4-oxo-2-(phenylamino)-(213273-03-1)
• EPA Substance Registry System: 4H-1-Benzopyran-3-carboxaldehyde, 4-oxo-2-(phenylamino)-(213273-03-1)

Safety Data

• Hazardous Substances Data: 213273-03-1(Hazardous Substances Data)

Upstream product

• 107-13-1 acrylonitrile 
• 113326-75-3 N-((4-oxo-4H-chromen-3-yl)methylene)aniline oxide 
• 79-06-1 2-propenamide 
• 109-92-2 ethyl vinyl ether 
• 118-93-4 o-hydroxyacetophenone 
• 122-79-2 Phenyl acetate 
• 108-95-2 phenol 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 17422-74-1 3-Formylchromone 
• 1219020-15-1 3-(ethylaminomethylene)-2-(N-phenyl)-iminochroman-4-one 
• 113326-75-3 C-(4-oxo-4H<1>benzopyran-3-yl)-N-phenylnitrone 
• 74143-89-8 5-phenyl-3,4-pentadien-2-one 
• 131431-64-6 ethyl hexa-2,3-dienoate 
• 74268-51-2 ethyl 2,3-pentadienecarboxylate 

Downstream Products

• 1173277-76-3 3,3'-methylenebis(2-N-phenylamino-4H-chromen-4-one) 
• 1170086-89-1 4-oxo-4H-chromene-3-carbothioic acid N-phenylamide 
• 1219020-12-8 2-(N-phenyl)imino-3-(p-tolylaminomethylene)-chroman-4-one 
• 1345096-79-8 3-(2-hydroxybenzoyl)-1-methylquinolin-2(1H)-one 
• 445291-56-5 2-(N-methyl-N-phenyl)aminochromone-3-carboxaldehyde 
• 52281-05-7 3-[(phenylamino)methylidene]-3,4-dihydro-2H-1-benzopyran-2,4-dione 
• 1535170-91-2 4-chloro-3-dichloromethyl-2-(N-phenyl)imino-2H-1-benzopyran 
• 1293279-24-9 6,8-di(N-phenylimino)-7H-pyrano[3,2-c:5,6-c']dicoumarin 
• 39079-64-6 4-oxo-N-phenyl-4H-1-benzopyran-3-carboxamide 
• 1246677-47-3 C₂₁H₁₉NO₃ 
• 445291-70-3 2-(o-anisylamino)-3-formylchromone 
• 445291-67-8 2-(p-anisylamino)-3-formylchromone 

Relevant articles and documents

Investigations on peri-, regio- and stereoselectivities in thermal cycloadditions involving C-(4-oxo-4H[1]benzopyran-3-yl)-N-phenylnitrones: Role of steric factors and secondary interactions in 1,3-dipolar cycloadditions

Complete peri-, regio- and stereoselectivities in thermal reactions of C-(4-oxo-4H[1]benzopyran-3-yl)-N-phenylnitrones with both electron-rich and electron-deficient olefins have been investigated. This conjugated nitrone undergoes frontier-orbital (LUMO-

Exploring α-chromonyl nitrones as 1,5-dipoles

N-Phenyl-C-chromonyl nitrones 1 and the allenoate zwitterion 2, generated by addition of phosphine to acetylenedicarboxylates, undergo a cascade reaction sequence involving an unprecedented [5+3] annulation followed by deoxygenative rearrangement leading to dihydropyridine-fused benzopyrones. Unusual electronic control by the N-substituents of 1 directs the annulation pathway, leading to two different ring-systems. Georg Thieme Verlag Stuttgart - New York.

Regio- and stereoselective synthesis of 1-benzopyrano[2,3-b]pyrrolo[2,3-d] pyridines: A microwave-accelerated intramolecular [3+2] cycloaddition reaction of azomethine ylide

Figure represented. Regio- and stereoselective syntheses of tetracyclic compounds having chromone, pyrrolidine, and piperidine rings have been accomplished by an intramolecular [3+2] cycloaddition reaction involving azomethine ylide. The reactions were ca