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thiobutabarbital
Sign in to saveThiobutabarbital (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.
Chemical data
- Formula
- C10H16N2O2S
- Molecular weight
- 228.31 g/mol
- IUPAC name
- 5-butan-2-yl-5-ethyl-2-sulfanylidene-1,3-diazinane-4,6-dione
- SMILES
- CCC(C)C1(C(=O)NC(=S)NC1=O)CC
- InChIKey
- IDELNEDBPWKHGK-UHFFFAOYSA-N
- XLogP
- 2.2
- Polar surface area
- 90.3 Ų
- H-bond donors
- 2
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 228.093
Show 4 more facts
- chemical formula
- C₁₀H₁₆N₂O₂S
- canonical SMILES
- CCC(C)C1(C(=O)NC(=S)NC1=O)CC
- medical condition treated
- insomnia
- Commons category
- Thiobutabarbital
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- Stereochemistry
- References
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.
== 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: {| class="wikitable" style="text-align:center" |- class="hintergrundfarbe6" ! colspan="2"| Enantiomers of Thiobutabarbital |- | 130 px (R)-Form | 130 px (S)-Form |}
Excerpted from Wikipedia’s “thiobutabarbital” article, available under the CC BY-SA 4.0 licence.