Acetoxyacetylaminofluorene

Acetoxyacetylaminofluorene

Names
IUPAC name [Acetyl(9H-fluoren-2-yl)amino] acetate[1]
Other names N-Acetoxy-2-acetamidofluorene;[1] N-Acetoxy-2-acetylaminofluorene;[1] Acetoxy AAF;[1] Acetoxyacetamidofluorene;[1] Acetoxyfluorenylacetamide;[1]
Identifiers
Abbreviations	NAAAF
CAS Registry Number	6098-44-8 N
ChEBI	CHEBI:234426 N
ChEMBL	ChEMBL85327 Y
ChemSpider	21074 Y
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 Y Key: NFOMHWALMFWNAQ-UHFFFAOYSA-N Y 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
Jmol-3D images	Image Image
MeSH	Acetoxyacetylaminofluorene
PubChem	22469
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
Molecular formula	C17H15NO3
Molar mass	281.31 g·mol−1
log P	3.327
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
N verify (what is: Y/N?)
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.

See also

• Hydroxyacetylaminofluorene

References