COC1=CC=CC(=C1)N1C(=O)NC(=O)C(C=NNC(=O)C2=CC=C(C=C2)[N+]([O-])=O)C1=O

InChIKey=AFIUYZZODFXEHG-UHFFFAOYSA-N

C19H15N5O7

425.357

Organic compounds

Organoheterocyclic compounds

Diazines

Pyrimidines and pyrimidine derivatives

Pyrimidones

Barbituric acid derivatives

Nitrobenzenes Benzoic acids and derivatives Phenoxy compounds Nitroaromatic compounds Methoxybenzenes Benzoyl derivatives Anisoles Alkyl aryl ethers Diazinanes 1,3-dicarbonyl compounds Dicarboximides Organic carbonic acids and derivatives Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxoanionic compounds Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Nitrobenzene - Benzoic acid or derivatives - Barbiturate - Phenoxy compound - Nitroaromatic compound - Methoxybenzene - Phenol ether - Benzoyl - Anisole - Alkyl aryl ether - Benzenoid - 1,3-dicarbonyl compound - 1,3-diazinane - Monocyclic benzene moiety - Dicarboximide - Organic nitro compound - Carbonic acid derivative - C-nitro compound - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Organic hyponitrite - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as barbituric acid derivatives. These are compounds containing a perhydropyrimidine ring substituted at C-2, -4 and -6 by oxo groups.

Not available