Salicylanilide

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by DePiep (talk | contribs) at 13:36, 2 November 2015 (Chembox: unknown parameters: fix spelling, replace or remove. See also full parameter list (via AWB script)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Salicylanilide[1]
Names
IUPAC name
2-Hydroxy-N-phenylbenzamide
Other names
2-Hydroxybenzanilide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.001.571 Edit this at Wikidata
UNII
  • InChI=1S/C13H11NO2/c15-12-9-5-4-8-11(12)13(16)14-10-6-2-1-3-7-10/h1-9,15H,(H,14,16) ☒N
    Key: WKEDVNSFRWHDNR-UHFFFAOYSA-N ☒N
  • InChI=1/C13H11NO2/c15-12-9-5-4-8-11(12)13(16)14-10-6-2-1-3-7-10/h1-9,15H,(H,14,16)
    Key: WKEDVNSFRWHDNR-UHFFFAOYAI
  • C1=CC=C(C=C1)NC(=O)C2=CC=CC=C2O
Properties
C13H11NO2
Molar mass 213.236 g·mol−1
Appearance White to off-white crystalline solid
Melting point 136 to 138 °C (277 to 280 °F; 409 to 411 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Salicylanilide is a chemical compound which is the amide of salicylic acid and aniline. It is classified as both a salicylamide and an anilide.[2]

Derivatives of salicylanilide have a variety of pharmacological uses. Chlorinated derivatives including niclosamide, oxyclozanide, and rafoxanide are used as anthelmintics, especially as flukicides. Brominated derivatives including dibromsalan, metabromsalan, and tribromsalan are used as disinfectants with antibacterial and antifungal activities.


USES- it can be use as anti septic agents.

References

  1. ^ salicylanilide at chemicalland21.com
  2. ^ Salicylanilides at the U.S. National Library of Medicine Medical Subject Headings (MeSH)