Thiobutabarbital
Chemical compound
- none
- 5-sec-butyl-5-ethyl-2-thioxodihydropyrimidine-4,6(1H,5H)-dione
- 2095-57-0
N
- 3032373
- 2297366
Y
- 2N0251U7JH
- Interactive image
- O=C1NC(=S)NC(=O)C1(C(C)CC)CC
InChI
- InChI=1S/C10H16N2O2S/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15)Y
- Key:IDELNEDBPWKHGK-UHFFFAOYSA-NY
N
Y (what is this?) (verify)Thiobutabarbital (Inactin, Brevinarcon) is a short-acting barbiturate derivative invented in the 1950s. It has sedative, anticonvulsant and hypnotic effects, and is still used in veterinary medicine for induction in surgical anaesthesia.[1]
Stereochemistry
Thiobutabarbital contains a stereocenter and consists of two enantiomers. This is a racemate, i.e. a 1: 1 mixture of ( R ) - and the ( S ) - form:[2]
| Enantiomers of Thiobutabarbital | |
|---|---|
 (R)-Form |  (S)-Form |
References
- ^ Rieg T, Richter K, Osswald H, Vallon V (October 2004). "Kidney function in mice: thiobutabarbital versus alpha-chloralose anesthesia". Naunyn-Schmiedeberg's Archives of Pharmacology. 370 (4): 320–3. doi:10.1007/s00210-004-0982-x. PMID 15549274. S2CID 25580831.
- ^ Entry on Thiobutabarbital. at: Römpp Online. Georg Thieme Verlag, retrieved 15. Juni 2014.
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