Acetoxyacetylaminofluorene

Acetoxyacetylaminofluorene
Names
	Preferred IUPAC name N-(Acetyloxy)-N-(9H-fluoren-2-yl)acetamide
	Other names N-Acetoxy-N-(9H-fluoren-2-yl)acetamide; N-Acetoxy-2-acetamidofluorene; N-Acetoxy-2-acetylaminofluorene; Acetoxyacetamidofluorene; Acetoxyfluorenylacetamide
Identifiers
CAS Number	6098-44-8 ;
3D model (JSmol)	Interactive image; Interactive image;
Abbreviations	NAAAF
ChEBI	CHEBI:234426 ;
ChEMBL	ChEMBL85327 ;
ChemSpider	21074 ;
MeSH	Acetoxyacetylaminofluorene
PubChem CID	22469;
UNII	Q3EAS7L4RW ;
CompTox Dashboard (EPA)	DTXSID90209828 ;
	InChI InChI=1S/C17H15NO3/c1-11(19)18(21-12(2)20)15-7-8-17-14(10-15)9-13-5-3-4-6-16(13)17/h3-8,10H,9H2,1-2H3 Key: NFOMHWALMFWNAQ-UHFFFAOYSA-N ; InChI=1/C17H15NO3/c1-11(19)18(21-12(2)20)15-7-8-17-14(10-15)9-13-5-3-4-6-16(13)17/h3-8,10H,9H2,1-2H3 Key: NFOMHWALMFWNAQ-UHFFFAOYAD;
	SMILES CC(=O)ON(C(C)=O)c1ccc-2c(Cc3ccccc-23)c1; CC(=O)ON(C(C)=O)C1=CC=C2C(CC3=C2C=CC=C3)=C1;
Properties
Chemical formula	C17H15NO3
Molar mass	281.311 g·mol−1
log P	3.327
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Acetoxyacetylaminofluorene is a derivative of 2-acetylaminofluorene used as a biochemical tool in the study of carcinogenesis. It forms adducts with DNA by reacting with guanine at its C-8 position.;^[1] This results in breaks in one strand of the DNA.

References

^ ^a ^b ^c ^d ^e CID 22469 from PubChem

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[PubChem-1] CID 22469 from PubChem

[1]

Acetoxyacetylaminofluorene

See also

References