Acetanilide - Wikipedia Acetanilide is the organic compound with the formula C 6 H 5 NHC(O)CH 3 It is the N-acetylated derivative of aniline [ 7 ] It is an odourless solid chemical of leaf or flake-like appearance
Acetanilide | C8H9NO | CID 904 - PubChem Acetanilide | C8H9NO | CID 904 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety hazards toxicity information, supplier lists, and more
Acetanilide - an overview | ScienceDirect Topics Moreover, other studies conducted according to present-day regulated guidelines are negative Taken together, acetanilide was considered to be non-clastogenic in the in vivo micronucleus test Based on the data available, acetanilide does not present a concern for genotoxic potential
Acetanilide | synthesis, analgesic, antipyretic | Britannica acetanilide, synthetic organic compound introduced in therapy in 1886 as a fever-reducing drug Its effectiveness in relieving pain was discovered soon thereafter, and it was used as an alternative to aspirin for many years in treating such common complaints as headache, menstrual cramps, and rheumatism
Acetanilide | 103-84-4 - ChemicalBook Acetanilide, a para-aminophenol derivative with analgesic, antipyretic and weak antiinflammatory activity, was introduced into medicine in 1886 It subsequently proved to be excessively myelosuppressive and has been superseded by safer alternatives
Acetanilide Formula, Preparation, Melting Point, Solubility, MSDS Acetanilide is a white solid organic compound mainly used in organic synthesis Other names of this compound include N-phenylacetamide, acetanilide and acetanil It was formerly used for treating fever and headache and was known by its brand name Antifebrin
ACETANILIDE | CAMEO Chemicals | NOAA ACETANILIDE is an amide Flammable gases are formed by the reaction of organic amides 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