Compounds similar to this structure
O=[N+]([O-])c1cc([N+](=O)[O-])c(NN(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1Edit in Covalent
200 compounds score at least 30 % on Tanimoto similarity of circular fingerprints, most similar first.
3,5-Dinitrosalicylaldehyde2460-59-537 % similar
6-Chloro-2-nitrobenzonitrile6575-07-137 % similar
4-Phenyl-2-nitrophenol885-82-537 % similar
2-Chloro-3,5-dinitrobenzoic acid2497-91-837 % similar
HC Red 12784-89-637 % similar
4-Chloro-3-nitrobenzophenone56107-02-937 % similar
Bis(2-nitrophenyl) disulfide1155-00-637 % similar
1-Fluoro-2-nitrobenzene1493-27-237 % similar
2,2′-Dinitrodibenzyl16968-19-737 % similar
1,2,3-Trichloro-5-nitrobenzene20098-48-037 % similar
1-Iodo-2-nitrobenzene609-73-437 % similar
2-Nitrotoluene88-72-237 % similar
2-Nitroaniline88-74-437 % similar
Nitrophenol88-75-537 % similar
4-Nitrobenzophenone1144-74-736 % similar
2-Bromo-1-chloro-3-nitrobenzene19128-48-436 % similar
2-Nitrophenyl phenyl sulfide4171-83-936 % similar
2-Chloro-6-nitrobenzenamine769-11-936 % similar
1-Chloro-2-methyl-3-nitrobenzene83-42-136 % similar
HC Yellow 24926-55-036 % similar
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