| Identification | Back Directory | [Name]
4-ACETAMIDOFLUORENE | [CAS]
28322-02-3 | [Synonyms]
4-AAF
N-4-Fluorenyl
4-ACETAMIDOFLUORENE
4-fluorenylacetamide
4-Acetylaminofluoren
4-Acetylaminofluorene
N-4-Fluorenylacetamide
n-fluoren-4-yl-acetamid
N-Fluoren-4-ylacetamide
4-ACETAMIDOFLUORENE 99%
N-4-ACETYLAMINOFLUORENE
acetamide,n-fluoren-4-yl
4-Acetylamino-9H-fluorene
Acetamide, N-fluoren-4-yl-
n-9h-fluoren-4-yl-acetamid
n-9h-fluoren-4-ylacetamide
acetamide,n-9h-fluoren-4-yl
4-(Acetylamino)-9H-fluorene
N-(9H-Fluoren-4-yl)acetamide | [EINECS(EC#)]
248-964-3 | [Molecular Formula]
C15H13NO | [MDL Number]
MFCD00027394 | [MOL File]
28322-02-3.mol | [Molecular Weight]
223.27 |
| Hazard Information | Back Directory | [Definition]
ChEBI: A member of the class of acetamides that is acetamide in which one of the hydrogens attached to the nitrogen is replaced by a 9H-fluoren-4-yl group. | [General Description]
Light beige powder. | [Air & Water Reactions]
Insoluble in water. | [Reactivity Profile]
An amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). | [Health Hazard]
ACUTE/CHRONIC HAZARDS: When heated to decomposition 4-ACETAMIDOFLUORENE emits toxic fumes of NOx. | [Fire Hazard]
Flash point data for 4-ACETAMIDOFLUORENE are not available; however, 4-ACETAMIDOFLUORENE is probably combustible. |
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