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TOMSO

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Find sources: "TOMSO" – news ·newspapers ·books ·scholar ·JSTOR
(December 2017)
Pharmaceutical compound
TOMSO
Clinical data
Other names2-Methoxy-4-methyl-5-methylsulfinylamphetamine
Routes of
administration
Oral[1]
ATC code
  • None
Pharmacokinetic data
Duration of action10–16 hours[1]
Identifiers
  • 1-[5-(methanesulfinyl)-2-methoxy-4-methylphenyl]propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H19NO2S
Molar mass241.35 g·mol−1
3D model (JSmol)
  • COC1=C(C=C(C(=C1)C)S(=O)C)CC(C)N
  • InChI=1S/C12H19NO2S/c1-8-5-11(15-3)10(6-9(2)13)7-12(8)16(4)14/h5,7,9H,6,13H2,1-4H3 checkY
  • Key:LMQLBXOYCGXTOM-UHFFFAOYSA-N checkY
  (verify)

TOMSO, also known as2-methoxy-4-methyl-5-methylsulfinylamphetamine, is adrug and asubstituted amphetamine.[1] TOMSO was first synthesized byAlexander Shulgin.[1] In his bookPiHKAL, the dose range is listed as 100–150 mg, and the duration is listed as 10–16 hours.[1] TOMSO is inactive on its own; it is activated with the consumption ofalcohol.[1] It produces intense time distortion and a threshold.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of TOMSO.[1]

See also

[edit]

References

[edit]
  1. ^abcdefghTOMSO entry inPiHKAL
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
Others
Natural sources
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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