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Methallatal

From Wikipedia, the free encyclopedia

Pharmaceutical compound
Methallatal
Clinical data
Trade namesMosidal
Identifiers
  • 5-ethyl-5-(2-methylprop-2-enyl)-2-sulfanylidene-1,3-diazinane-4,6-dione
CAS Number
PubChemCID
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.003.723Edit this at Wikidata
Chemical and physical data
FormulaC10H14N2O2S
Molar mass226.29 g·mol−1
3D model (JSmol)
  • CCC1(C(=O)NC(=S)NC1=O)CC(=C)C
  • InChI=1S/C10H14N2O2S/c1-4-10(5-6(2)3)7(13)11-9(15)12-8(10)14/h2,4-5H2,1,3H3,(H2,11,12,13,14,15)
  • Key:XMQICEWOKPEQRG-UHFFFAOYSA-N

Methallatal is abarbiturate derivative first synthesized in the 1940s (designationV-12).[1][2] It hassedative andhypnotic properties.

Methallatal was formerly marketed under the trade nameMosidal from 1940s to 1950s forveterinary use, specifically for preventingmotion sickness indogs.[2]

References

[edit]
  1. ^Carson GB (1954).The barbiturates in forensic chemistry.Ohio State University. Retrieved2026-02-11.
  2. ^abElliott KA, Noble RL (September 1948)."Control of car sickness in a dog by V-12 (mosidal)".Canadian Medical Association Journal.59 (3): 277.PMC 1591212.PMID 18877437.
Alcohols
Barbiturates
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Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
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