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This article relies largely or entirely on a single source. Relevant discussion may be found on the talk page. Please help improve this article by introducing citations to additional sources. Find sources: "TOMSO" – news · newspapers · books · scholar · JSTOR (December 2017)

TOMSO

Names
Preferred IUPAC name 1-propan-2-amine
Identifiers
CAS Number	757142-16-8
3D model (JSmol)	Interactive image
ChemSpider	21106387
PubChem CID	15915373
UNII	7SW3C48M3B
CompTox Dashboard (EPA)	DTXSID901027145
InChI InChI=1S/C12H19NO2S/c1-8-5-11(15-3)10(6-9(2)13)7-12(8)16(4)14/h5,7,9H,6,13H2,1-4H3Key: LMQLBXOYCGXTOM-UHFFFAOYSA-N InChI=1/C12H19NO2S/c1-8-5-11(15-3)10(6-9(2)13)7-12(8)16(4)14/h5,7,9H,6,13H2,1-4H3Key: LMQLBXOYCGXTOM-UHFFFAOYAD
SMILES COC1=C(C=C(C(=C1)C)S(=O)C)CC(C)N
Properties
Chemical formula	C12H19NO2S
Molar mass	241.35 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is  ?) Infobox references

TOMSO (2-methoxy-4-methyl-5-methylsulfinylamphetamine) is a lesser-known psychedelic drug and a substituted amphetamine. TOMSO was first synthesized by Alexander Shulgin. In his book PiHKAL, the dosage range is listed as 100–150 mg, and the duration listed as 10–16 hours. TOMSO is inactive on its own; it is activated with the consumption of alcohol. It produces intense time distortion and a threshold. Very little data exists about the pharmacological properties, metabolism, and toxicity of TOMSO.

See also

• TOM (psychedelic)

References

1. TOMSO entry in PiHKAL

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