Fenozolone

Fenozolone
Skeletal formula
Space-filling model of fenozolone
Clinical data
Routes of
administration		Oral
ATC code
Identifiers
IUPAC name
  • (RS)-2-ethylamino-5-phenyl-1,3-oxazol-4-one
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
ECHA InfoCard100.035.747
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Chemical and physical data
FormulaC11H12N2O2
Molar mass204.229 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
SMILES
  • O=C1\N=C(/OC1c2ccccc2)NCC
InChI
  • 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) checkY
  • Key:RXOIEVSUURELPG-UHFFFAOYSA-N checkY
  (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. Zeitschrift für Klinische Chemie und Klinische Biochemie. 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.


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