Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	64935
Common Name:	2-nitroimidazole
Systematic Name:	2-nitro-1H-imidazole
RefMet Name:	2-Nitroimidazole
Synonyms:	2-nitroimidazole; Amicin; Azomycin; nitroimidazole [PubChem Synonyms]
Exact Mass:	113.0225 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C3H3N3O2
InChIKey:	YZEUHQHUFTYLPH-UHFFFAOYSA-N
ClassyFire superclass:	Organic 1,3-dipolar compounds [C0003630]
ClassyFire class:	Allyl-type 1,3-dipolar organic compounds [C0003631]
ClassyFire subclass:	Organic nitro compounds [C0001152]
ClassyFire direct parent:	Nitroaromatic compounds [C0004612]
NP-MRD NMR spectra:	View NMR spectra
SMILES:	c1cnc([nH]1)[N+](=O)[O-]
Studies:	Available studies (via RefMet name)

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References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y