Acetanilide - Wikipedia
Acetanilide is the organic compound with the formula C6H5NHC (O)CH3. It is the N-acetylated derivative of aniline. [7] It is an odourless solid chemical of leaf or flake-like appearance. It is also known as N-phenylacetamide, acetanil, or acetanilid, and …
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 | 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 - Wikiwand
Acetanilide is the organic compound with the formula C6H5NHC (O)CH3. It is the N-acetylated derivative of aniline. It is an odourless solid chemical of leaf or flake-like appearance. It is also known as N-phenylacetamide, acetanil, or acetanilid, and …
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 | C8H9NO - ChemSpider
ChemSpider record containing structure, synonyms, properties, vendors and database links for Acetanilide, 103-84-4.
Acetanilide - an overview | ScienceDirect Topics
Acetaminophen (paracetamol) was developed as a derivative of acetanilide, which was discovered serendipitously to have antipyretic properties when it was mistakenly used as an anti-helminthic agent in the late 19th century in Germany.
Acetanilide - an overview | ScienceDirect Topics
Acetanilides are selective preemergence herbicides that interfere with root development by electrophilic inhibition of the fatty acid synthetic enzyme elongase (Hock and Elstner, 2004). The skin effects of these compounds are quite similar, reflecting the high degree of similarity in their chemical structures.
Acetanilide | The Merck Index Online - Royal Society of Chemistry
How can I get access to The Merck Index* Online? Institutions wanting access to The Merck Index* Online should contact [email protected] or their local Royal Society of Chemistry representative to find out more. rsc.org.
Acetamide, N-phenyl- - NIST Chemistry WebBook
Acetamide, N-phenyl-. Formula: C 8 H 9 NO. Molecular weight: 135.1632. IUPAC Standard InChI: InChI=1S/C8H9NO/c1-7 (10)9-8-5-3-2-4-6-8/h2-6H,1H3, (H,9,10) Copy Sheet of paper on top of another sheet. IUPAC Standard InChIKey: FZERHIULMFGESH-UHFFFAOYSA-N. Copy Sheet of paper on top of another sheet.