OCCN1CCN(CC1)C1=C(C(=NC=N1)N(CC1=CC=CC=C1)C1=CC=CC=N1)[N+]([O-])=O

InChIKey=HGSLBUHELNKVCU-UHFFFAOYSA-N

C22H25N7O3

435.488

Organic compounds

Benzenoids

Benzene and substituted derivatives

Benzylamines

Not available

2-benzylaminopyridines

Alkyldiarylamines N-arylpiperazines Dialkylarylamines Nitroaromatic compounds Aminopyridines and derivatives Aminopyrimidines and derivatives N-alkylpiperazines Imidolactams Heteroaromatic compounds Trialkylamines 1,2-aminoalcohols Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Primary alcohols Organic salts Organic zwitterions Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

2-benzylaminopyridine - N-arylpiperazine - Alkyldiarylamine - Nitroaromatic compound - Dialkylarylamine - Aminopyridine - Aminopyrimidine - N-alkylpiperazine - 1,4-diazinane - Piperazine - Pyridine - Pyrimidine - Imidolactam - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Tertiary amine - Tertiary aliphatic amine - 1,2-aminoalcohol - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Alkanolamine - Organoheterocyclic compound - Allyl-type 1,3-dipolar organic compound - Azacycle - Organic oxoazanium - Organic salt - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organic zwitterion - Alcohol - Amine - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as 2-benzylaminopyridines. These are aromatic compounds containing pyridine ring substituted at the 2-position by a benzylamine group.

Not available