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CAS No 76-68-6 , 2,4,6(1H,3H,5H)-Pyrimidinetrione,5-(2-cyclopenten-1-yl)-5-(2-propen-1-yl)-

  • Name: 2,4,6(1H,3H,5H)-Pyrimidinetrione,5-(2-cyclopenten-1-yl)-5-(2-propen-1-yl)-
  • Synonyms: Barbituric acid,5-allyl-5-(2-cyclopenten-1-yl)- (6CI,7CI,8CI); Allylcyclopentenylbarbital; Cyclopental; Dormisan;5-Allyl-5-(1-cyclopentenyl-2)barbituric acid;2,4,6(1H,3H,5H)-Pyrimidinetrione,5-(2-cyclopenten-1-yl)-5-(2-propen-1-yl)-;Allylpental; Cyclopentobarbital; Cyclopen; Ciclopal; Cyclopentenylallylbarbituricacid;2,4,6(1H,3H,5H)-Pyrimidinetrione,5-(2-cyclopenten-1-yl)-5-(2-propenyl)- (9CI); Cyclopal;5-Allyl-5-(2-cyclopenten-1-yl)barbituric acid; Cyclopentobarbitone;
  • CAS Registry Number:
  • Transport: 3249
  • Density: 1.224g/cm3
  • Refractive index: 1.538
  • EINECS: 200-979-6
  • Molecular Weight: 234.25116
  • InChI: InChI=1/C12H14N2O3/c1-2-7-12(8-5-3-4-6-8)9(15)13-11(17)14-10(12)16/h2-3,5,8H,1,4,6-7H2,(H2,13,14,15,16,17)
  • Molecular Formula: C12H14 N2 O3
  • Molecular Structure:CAS No:76-68-6 2,4,6(1H,3H,5H)-Pyrimidinetrione,5-(2-cyclopenten-1-yl)-5-(2-propen-1-yl)-

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References of 2,4,6(1H,3H,5H)-Pyrimidinetrione,5-(2-cyclopenten-1-yl)-5-(2-propen-1-yl)-
Title: Cyclopentobarbital
CAS Registry Number: 76-68-6
CAS Name: 5-(2-Cyclopenten-1-yl)-5-(2-propenyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
Synonyms: 5-allyl-5-(2-cyclopenten-1-yl)barbituric acid
Trademarks: Cyclopal (Kytta-Siegfried)
Molecular Formula: C12H14N2O3
Molecular Weight: 234.25
Percent Composition: C 61.53%, H 6.02%, N 11.96%, O 20.49%
Literature References: Prepd by condensing the ethyl ester of cyclopentenylmalonic acid with urea: Compagnie de Bethune: DE 589947 (1930), Frdl. 19, 1198; GB 349455; FR 38680.
Properties: Crystals, mp 139-140°. Bitter taste. Slightly sol in cold water; moderately sol in hot water. Freely sol in alcohol, organic solvents.
Melting point: mp 139-140°
NOTE: This is a controlled substance (depressant): 21 CFR, 1308.13.
Therap-Cat: Sedative, hypnotic.
Keywords: Sedative/Hypnotic; Barbituric Acid Derivatives.
 
 
Status: This monograph has been retired and is no longer subject to revision or update.