Acetamide, N-9H-fluoren-2-yl-

PubChem Notes:

2-Acetylaminofluorene A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.

Molecular Formula: C15H13NO


InChI: InChI=1/C15H13NO/c1-10(17)16-13-6-7-15-12(9-13)8-11-4-2-3-5-14(11)15/h2-7,9H,8H2,1H3,(H,16,17)/f/h16H

InChIKey: InChIKey=CZIHNRWJTSTCEX-WYUMXYHSCF
SMILES: CC(=O)Nc1ccc-2c(Cc3ccccc-23)c1

CAS number 53-96-3

Names:
    Acetamide, N-9H-fluoren-2-yl-
    N-fluoren-2-ylacetamide
    N-(9H-fluoren-2-yl)acetamide
    N-2-Fluorenylacetamide
    2-AAF
    2-Acetamidofluorene
    2-acetamidofluorene
    2-FAA

Registries:
    PubChem CID 5897
    Beilstein =2807677
    CAS 53-96-3 (from NIST)
    ChEBI 17356
    Kegg C02778
    PubChem ID 10437940
    PubChem ID 5729