Fenozolone

Last updated
Fenozolone
Fenozolone.svg
Fenozolone molecule spacefill.png
Clinical data
Routes of
administration
Oral
ATC code
Identifiers
  • (RS)-2-ethylamino-5-phenyl-1,3-oxazol-4-one
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.035.747 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C11H12N2O2
Molar mass 204.229 g·mol−1
3D model (JSmol)
Chirality Racemic mixture
  • O=C1\N=C(/OC1c2ccccc2)NCC
  • InChI=1S/C11H12N2O2/c1-2-12-11-13-10(14)9(15-11)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H,12,13,14) Yes check.svgY
  • Key:RXOIEVSUURELPG-UHFFFAOYSA-N Yes check.svgY
   (verify)

Fenozolone (Ordinator) was developed by Laboratoires Dausse in the 1960s [1] and is a psychostimulant related to pemoline. [2]

See also

References

  1. DE 1297108,Beil W, Hoeppener A, Wolff HJ,"5-phenyl-2-ethylamino-4-oxazolinone and its preparation",issued 12 June 1969, assigned to Les Laboratoires Dausse SA
  2. Gielsdorf W (February 1982). "Determination of the psychostimulants pemoline, fenozolone and thozalinone in human urine by gas chromatography/mass spectrometry and thin layer chromatography". Journal of Clinical Chemistry and Clinical Biochemistry. 20 (2): 65–8. doi:10.1515/cclm.1982.20.2.65. PMID   6121837. S2CID   38935748. Archived from the original on 2021-05-31. Retrieved 2021-05-31.