Weight | 208.217 g/mol |
---|---|
Formula | C10H12N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 4 |
ALLOBARBITAL (52-43-7)
diallylbarbituric acid · diallyl barbituric acid · allobarbitone
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- Enhancement of hepatocarcinogenesis and induction of specific cytochrome P450-dependent monooxygenase activities by the barbiturates allobarbital, aprobarbital, pentobarbital, secobarbital and 5-phenyl- and 5-ethylbarbituric acids (Carcinogenesis, 1994)
- Anaesthetic Properties of Some New Nsubstituted and N,N' disubstituted Derivatives of 5,5DiallylBarbituric Acid. (Acta Physiologica Scandinavica, 1951)
- Reduction of Barbituric Acids with Sodium Borohydride. Reduction of 5,5-Diallyl-1-methylbarbituric Acid. (Acta Chemica Scandinavica, 1979)
- Etude thermoanalytique de substances psychotropes: V. Barbital et allobarbital (Thermochimica Acta, 1986)
- Structure of 5,5-diallyl-1-(p-bromophenyl)barbituric acid (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1980)
- The Distribution of Calcium Between Blood and Cerebrospinal Fluid in Sleep Induced by Diallyl-Barbituric Acid (Journal of Nervous and Mental Disease, 1932)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - diallylbarbituric acid
- diallyl barbituric acid
- allobarbitone
- 5,5-diallylbarbituric acid
- diallylmal
- diallylbarbital
-
SMILESC=CCC1(C(=O)NC(=O)NC1=O)CC=C
-
InChIKeyFDQGNLOWMMVRQL-UHFFFAOYSA-N
- Pubchem - ALLOBARBITAL
- Wikipedia - allobarbital
Allobarbital, also known as allobarbitone and branded as Cibalgine or Dial-Ciba (in combination with ethyl carbamate), is a barbiturate derivative invented in 1912 by Ernst Preiswerk and Ernst Grether working for CIBA. It was used primarily as an anticonvulsant although it has now largely been replaced by newer drugs with improved safety profiles. Other uses for allobarbital included as an adjutant to boost the activity of analgesic drugs, and use in the treatment of insomnia and anxiety.
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