Salicylanilide

Salicylanilide[1]
Names
Preferred IUPAC name
2-Hydroxy-N-phenylbenzamide
Other names
2-Hydroxybenzanilide
Identifiers
CAS Number
  • 87-17-2 checkY
3D model (JSmol)
  • Interactive image
Beilstein Reference
1108135
ChEBI
  • CHEBI:239133
ChEMBL
  • ChEMBL82970
ChemSpider
  • 6610 checkY
ECHA InfoCard 100.001.571 Edit this at Wikidata
EC Number
  • 201-727-8
KEGG
  • C18915
PubChem CID
  • 6872
UNII
  • LHP8NEY345 checkY
CompTox Dashboard (EPA)
  • DTXSID7021784 Edit this at Wikidata
InChI
  • 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
Chemical formula
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)
Hazards
GHS labelling:[2]
Pictograms
GHS07: Exclamation markGHS09: Environmental hazard
Warning
Hazard statements
H315, H319, H335, H400
Precautionary statements
P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P391, P403+P233, P405, P501
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 ?)
Infobox references
Chemical compound

Salicylanilide is a chemical compound which is the amide of salicylic acid and aniline. It is classified as both a salicylamide and an anilide.[3]

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

Salicylanilides may be used as antiseptics.

References

  1. ^ Salicylanilide at chemicalland21.com
  2. ^ "Salicylanilide". pubchem.ncbi.nlm.nih.gov. Retrieved 13 December 2021.
  3. ^ Salicylanilides at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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