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Furylfuramide
IUPAC name	(Z)-2-(2-furyl)-3-(5-nitro-2-furyl)prop-2-enamide
Other names	Tofuron, Alpha-2-furyl-5-nitro-2-furanacrylamide, 2-(2-Furyl)-3-(5-nitro-2-furyl)acrylic acid amide, a-(Furyl)-b-(5-nitro-2-furyl)acrylic amide, trans-2-(2-Furyl)-3-(5-nitro-2-furyl)acrylamide, 2-(2-furyl)-3-(5-nitro-2-furyl) acrylamide, 2-Furanacetamide, alpha-((5-nitro-2-furanyl)methylene)- [1],[2]
Abbreviations	AF-2, FF
Identifiers
CAS number	3688-53-7
PubChem	5280707
SMILES	C1=COC(=C1)C(=CC2=CC=C(O2)[N+](=O)[O-])C(=O)N
Properties
Molecular formula	C11H8N2O5
Molar mass	248.19162
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Furylfuramide is a synthetic nitrofuran derivative which was widely used as a food preservative in Japan since at least 1965, but withdrawn from the market in 1974 when it was observed to be mutagenic to bacteria in vitro and thus suspected of carcinogenicity. This was confirmed later when animal testing^[3] found it to cause benign and malignant tumors in the mammary glands, stomachs, esophagi, and lungs of rodents of both sexes, although insufficient evidence exists in human exposure.^[2]

This successful use of bacterial mutagenicity as a screen for carcinogenicity confirmed the use of this methodology as a rapid and efficient test, in comparison to animal testing alone, and led to its further development. The availability of such simpler tests in turn gave rise to greater government oversight and testing of compounds to which the public would be exposed.^[4]

References