3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline
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![3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/e12950926316471391dc800b1e861ec3.png "3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline")
3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline
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CAS No:
115044-40-1
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Formula:
C11H9N5O2
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Chemical Name:
3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline
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Synonyms:
3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline;3H-Imidazo[4,5-f]quinoxaline,3,8-dimethyl-2-nitro-;3H-Imidazo(4,5-f)quinoxaline, 3,8-dimethyl-2-nitro-;3,8-Dimethyl-2-nitro-3H-imidazo(4,5-f)quinoxaline;3,8-dimethyl-2-nitroimidazo[4,5-f]quinoxaline;ACMC-20e23v;CTK4A9142;DTXSID70150940;ZINC22058107;AKOS030255889
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CAS No:
Characteristics
89.4
1.5
1.59±0.1 g/cm3(Predicted)
257-258.5°C
495.9±55.0 °C(Predicted)
253.7ºC
1.778
5.68E-10mmHg at 25°C
3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline Use and Manufacturing
IQ-type carcinogens found in cooked food are biotransformed and bind to DNA through sequential N2-hydroxylation and O-esterification.The 2-nitro analoges may serve as anintermediate in the chemical synthesis to the metabolites.The metabolites are used instudies with nucleic acids for understanding the molecular aspects of the mutagenic action of these compounds.
3,8-Dimethyl-2-nitro-3H-imidazo[4,5-F]quinoxaline
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