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2. pubchem.ncbi.nlm.nih.gov › compound › acetanilAcetanilide | C8H9NO | CID 904 - PubChem

   pubchem.ncbi.nlm.nih.gov › compound › acetanil

   Acetanilide | C8H9NO | CID 904 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

3. en.wikipedia.org › wiki › AcetanilideAcetanilide - Wikipedia

   en.wikipedia.org › wiki › Acetanilide

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   Acetanilide is an odourless solid chemical of leaf or flake-like appearance. It is also known as N -phenylacetamide , acetanil , or acetanilid , and was formerly known by the trade name Antifebrin .

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     Acetanilide Structure, Formula & Properties

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     Bromination of Acetanilide | Mechanism & Steps

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     Hydrolysis of Acetanilide: Mechanism & Explanation

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5. www.chemspider.com › Chemical-StructureAcetanilide | C8H9NO | ChemSpider

   www.chemspider.com › Chemical-Structure

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   Acetanilide. Molecular Formula C 8 H 9 NO; Average mass 135.163 Da; Monoisotopic mass 135.068420 Da; ChemSpider ID 880

6. pubchem.ncbi.nlm.nih.gov › compound › Acetanilide-13C6Acetanilide-13C6 | C8H9NO | CID 12199320 - PubChem

   pubchem.ncbi.nlm.nih.gov › compound › Acetanilide-13C6

   Acetanilide-13C6 | C8H9NO | CID 12199320 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

7. pubchem.ncbi.nlm.nih.gov › 4_-Bromoacetanilide4'-Bromoacetanilide | C8H8BrNO | CID 7683 - PubChem

   pubchem.ncbi.nlm.nih.gov › 4_-Bromoacetanilide

   4'-Bromoacetanilide | C8H8BrNO | CID 7683 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

8. webbook.nist.gov › cgi › cbookAcetamide, N-phenyl- - NIST Chemistry WebBook

   webbook.nist.gov › cgi › cbook

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   IUPAC Standard InChIKey: FZERHIULMFGESH-UHFFFAOYSA-N. Copy Sheet of paper on top of another sheet. CAS Registry Number: 103-84-4. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file. The 3d structure may be viewed using Java or Javascript .

9. People also ask

   Is acetanilide a solid?

   • Computed by PubChem 2.2 (PubChem release 2021.10.14) Acetanilide is a white to gray solid. (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.

   Acetanilide | C8H9NO | CID 904 - PubChem

   pubchem.ncbi.nlm.nih.gov/compound/acetanilide

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   Is acetanilide an amide?

   • Amines, Aromatic 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.

   Acetanilide | C8H9NO | CID 904 - PubChem

   pubchem.ncbi.nlm.nih.gov/compound/acetanilide

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   Is acetanilide toxic?

   • Unfortunately, Acetanilide exhibited an unacceptable profile of toxic effects, the most alarming being cyanosis due to methemoglobinemia. The toxic profile prompted the search for supposedly less toxic aniline derivatives such as phenacetin.

   ACETANILIDE - Inxight Drugs

   drugs.ncats.io/substance/SP86R356CC

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   Is acetanilide a vapor?

   • ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere (1), acetanilide, which has an extrapolated vapor pressure of 1.2X10-3 mm Hg at 25 °C (2,SRC), will exist solely as a vapor in the ambient atmosphere.

   Acetanilide | C8H9NO | CID 904 - PubChem

   pubchem.ncbi.nlm.nih.gov/compound/acetanilide

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10. drugs.ncats.io › substance › SP86R356CCACETANILIDE - National Center for Advancing Translational ...

    drugs.ncats.io › substance › SP86R356CC

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    Acetanilide is a synthetic organic compound introduced clinically 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 headaches, menstrual cramps, and rheumatism.