28322-02-3 Usage
Description
4-ACETAMIDOFLUORENE, also known as N-(9H-fluoren-4-yl)acetamide, is a member of the acetamides class. It is characterized by a light beige powder appearance and is defined as an acetamide in which one of the hydrogens attached to the nitrogen is replaced by a 9H-fluoren-4-yl group. This chemical compound has potential applications in various industries due to its unique structure and properties.
Uses
Used in Chemical Synthesis:
4-ACETAMIDOFLUORENE is used as an intermediate in the synthesis of various organic compounds, particularly those involving the 9H-fluoren-4-yl group. Its unique structure allows for the creation of a wide range of molecules with diverse applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-ACETAMIDOFLUORENE is used as a building block for the development of new drugs. Its structural properties make it a valuable component in the design and synthesis of novel therapeutic agents, potentially targeting a variety of medical conditions.
Used in Research and Development:
4-ACETAMIDOFLUORENE is also utilized in research and development settings, where it serves as a key compound for studying the properties and behavior of acetamides and related chemical groups. This helps scientists better understand the underlying mechanisms of various chemical reactions and processes, ultimately contributing to the advancement of scientific knowledge in the field.
Used in Material Science:
In the field of material science, 4-ACETAMIDOFLUORENE may be employed in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its unique structure can contribute to the creation of advanced materials with potential applications in various industries, including electronics, coatings, and adhesives.
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.
Safety Profile
Poison by intraperitoneal route. Questionable carcinogen with experimental tumorigenic data. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx,.
Check Digit Verification of cas no
The CAS Registry Mumber 28322-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,2 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28322-02:
(7*2)+(6*8)+(5*3)+(4*2)+(3*2)+(2*0)+(1*2)=93
93 % 10 = 3
So 28322-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO/c1-10(17)16-14-8-4-6-12-9-11-5-2-3-7-13(11)15(12)14/h2-8H,9H2,1H3,(H,16,17)
