[NH4+].CN1C([O-])=C(N=C2C(=O)N(C)C(=O)N(C)C2=O)C(=O)N(C)C1=O

InChIKey=BBINVVWBDJPLOG-UHFFFAOYSA-N

C12H16N6O6

340.296

Organic compounds

Organoheterocyclic compounds

Diazines

Pyrimidines and pyrimidine derivatives

Pyrimidones

Barbituric acid derivatives

N-acyl ureas Diazinanes Hydropyrimidines Azomethines Vinylogous amides Dicarboximides Heteroaromatic compounds Vinylogous acids Secondary ketimines Lactams Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Organopnictogen compounds

Aromatic heteromonocyclic compounds

Barbiturate - N-acyl urea - Ureide - 1,3-diazinane - Hydropyrimidine - Azomethine - Dicarboximide - Secondary ketimine - Vinylogous acid - Vinylogous amide - Heteroaromatic compound - Ketimine - Lactam - Carbonic acid derivative - Urea - Azacycle - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Organic zwitterion - Carbonyl group - Imine - Organopnictogen compound - Organic oxygen compound - Organic salt - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - 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