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Butallylonal

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Butallylonal
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
  • 5-sec-Butyl-5-(beta-bromoallyl)barbituric acid
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.013.215Edit this at Wikidata
Chemical and physical data
FormulaC11H15BrN2O3
Molar mass303.156 g·mol−1
3D model (JSmol)
  • O=C1NC(=O)NC(=O)C1(C(C)CC)CC(\Br)=C
  • InChI=1S/C11H15BrN2O3/c1-4-6(2)11(5-7(3)12)8(15)13-10(17)14-9(11)16/h6H,3-5H2,1-2H3,(H2,13,14,15,16,17) checkY
  • Key:FWZMBTIUIQUJFF-UHFFFAOYSA-N checkY
  (verify)

Butallylonal is abarbiturate derivative invented in the 1920s.[1] It hassedative properties, and was used primarily as an anaesthetic inveterinary medicine.[2] Butallylonal is considered similar in effects topentobarbital but is longer in action, being considered an intermediate-acting barbiturate rather than short-acting.

References

[edit]
  1. ^US 1739662 
  2. ^Mittmann U, Schmidt HD, Schmier J, Wirth RH (1976). "Hemorrhagic shock with fixed hypotension and with spontaneous recovery of blood pressure. A comparison of two shock models".Basic Research in Cardiology.71 (1):47–59.doi:10.1007/BF01907782.PMID 1259685.S2CID 5567045.
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