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TOMSO

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(December 2017)
TOMSO
Names
Preferred IUPAC name
1-[5-(Methanesulfinyl)-2-methoxy-4-methylphenyl]propan-2-amine
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • 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
  • InChI=1/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
    Key: LMQLBXOYCGXTOM-UHFFFAOYAD
  • COC1=C(C=C(C(=C1)C)S(=O)C)CC(C)N
Properties
C12H19NO2S
Molar mass241.35 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

TOMSO (2-methoxy-4-methyl-5-methylsulfinylamphetamine) is a lesser-knownpsychedelic drug and asubstituted amphetamine. TOMSO was first synthesized byAlexander Shulgin. In his bookPiHKAL, the dosage 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. It produces intense time distortion and a threshold. Very little data exists about the pharmacological properties, metabolism, and toxicity of TOMSO.

See also

References

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
MDxx
FLY
25x-NB
(NBOMes and related)
Others
Cyclized
Lysergamides
Others
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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