Allobarbital

CAS: 52-43-7

Ref. TR-A544500

Product Information

• Name: Allobarbital
• Synonyms: 5,5-Diallybarbituric acid, 5,5-Di-2-propenyl-2,4,6(1H,3H,5H)pyrimidinetrione, Allobarbitone, Dial, 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-di-2-propen-1-yl-, 5,5-Di-2-propen-1-yl-2,4,6(1H,3H,5H)-pyrimidinetrione, 5,5-Di-2-propenyl-2,4,6-(1H,3H,5H)-pyrimidinetrione, 5,5-Diallylbarbiturate, 5,5-Diallylbarbituric acid, 5,5-Diallylpyrimidine-2,4,6-trione, Allylbarbitural, Alnox, Alobarbital, Barballyl, Barbidal, Barbituric acid, 5,5-diallyl-, Curral, Diadol, Dial (barbiturate), Diallylbarbital, Diallylbarbituric acid, Diallymal, Dorm, Dormallyl, Malil, Malilum, Novallyl, Nsc 9324, 5,5-di(prop-2-en-1-yl)pyrimidine-2,4,6(1H,3H,5H)-trione, 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-di-2-propenyl-, 5,5-Diallylbarbitursaeure, AI3-02725, 1,3-diprop-2-en-1-ylpyrimidine-2,4,6(1H,3H,5H)-trione, Allobarbitalum, Dialog, Diallylbarbiturate, Allbarbital, Allobarbitale, Diallymalum, 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-di-2-propenyl-

Description

Applications Allobarbital is a barbiturate derivative that is primarily used as an anticonvulsant. Allobarbital also shows hypnotic activity and is used to boost the activity of analgesic drugs. Studies show that Allobarbital is an effective promoters of hepatocarcinogenesis. Allobarbital is a Controlled Substance.
References Tateoka, Y. et al.: Yakug. Zas., 106, 504 (1986); Crawford, J.M. et al.: Neuropharmacology, 9, 31 (1970); Rice, J.M. et al.: Carcinogenesis, 15, 395 (1994);

• Brand: TRC

Chemical properties

• Molecular weight: 208.21
• Formula: C₁₀H₁₂N₂O₃
• Color/Form: White
• InChI: InChI=1S/C10H12N2O3/c1-3-5-10(6-4-2)7(13)11-9(15)12-8(10)14/h3-4H,1-2,5-6H2,(H2,11,12,13,14,15)
• SMILES: CC(C)=NNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]