[Rh++].[Rh++].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O.NCC(O)CN1C=CN=C1[N+]([O-])=O

InChIKey=RKDRVJFOQOJTFB-UHFFFAOYSA-J

C14H22N4O11Rh2

628.158

Organic compounds

Organic 1,3-dipolar compounds

Allyl-type 1,3-dipolar organic compounds

Organic nitro compounds

C-nitro compounds

Nitroaromatic compounds

N-substituted imidazoles Heteroaromatic compounds Acetate salts Secondary alcohols 1,2-aminoalcohols Propargyl-type 1,3-dipolar organic compounds Organic transition metal salts Organic oxoazanium compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic zwitterions Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds

Not available

Nitroaromatic compound - N-substituted imidazole - Heteroaromatic compound - Acetate salt - Imidazole - Azole - Secondary alcohol - Carboxylic acid salt - 1,2-aminoalcohol - Azacycle - Organic transition metal salt - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic zwitterion - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as nitroaromatic compounds. These are c-nitro compounds where the nitro group is C-substituted with an aromatic group.

Not available