CC1=NN(C(=O)C1=CC1=CC2=C(OC(=O)C3=C2C(C)=C(C)N=C3N)C=C1)C1=CC=C(C=C1)[N+]([O-])=O

InChIKey=UMBCZANNQHNERF-UHFFFAOYSA-N

C25H19N5O5

469.457

Organic compounds

Organoheterocyclic compounds

Benzopyrans

1-benzopyrans

Not available

Chromenopyridines

Coumarins and derivatives Nitrobenzenes Nitroaromatic compounds Aminopyridines and derivatives Pyranones and derivatives Methylpyridines Pyrazolones Imidolactams Vinylogous amides Heteroaromatic compounds Lactones Amino acids and derivatives Oxacyclic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organic salts Organic zwitterions Primary amines Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

Chromenopyridine - Coumarin - Nitrobenzene - Nitroaromatic compound - Aminopyridine - Methylpyridine - Pyranone - Monocyclic benzene moiety - Pyran - Pyrazolinone - Pyridine - Imidolactam - Benzenoid - Heteroaromatic compound - Pyrazoline - Vinylogous amide - Organic nitro compound - Amino acid or derivatives - Lactone - C-nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic oxoazanium - Organic salt - Amine - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Primary amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organic zwitterion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as chromenopyridines. These are aromatic heterocyclic compounds structurally characterized by a pyridine ring fused to a chromene moiety.

Not available