Anodyne

Aleph-6
2,5-Dimethoxy-4-phenylthioamphetamine
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC17H21NO2S[1]
Molecular mass303.4 g/mol[1]
Predicted LogP3.7[1]
Chiralityracemic[2]
Identifiers
[]
IUPAC name1-(2,5-dimethoxy-4-phenylsulfanylphenyl)propan-2-amine[1]
SMILESCC(CC1=CC(=C(C=C1OC)SC2=CC=CC=C2)OC)N[1]
InChIInChI=1S/C17H21NO2S/c1-12(18)9-13-10-16(20-3)17(11-15(13)19-2)21-14-7-5-4-6-8-14/h4-8,10-12H,9,18H2,1-3H3[1]
InChIKeyCSOTVYXYZSJOFL-UHFFFAOYSA-N[1]
Dosing

2,5-Dimethoxy-4-phenylthioamphetamine

2,5-Dimethoxy-4-phenylthioamphetamine (also known as 2,5-Dimethoxy-α-methyl-4-(phenylthio)benzeneethanamine, Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-(phenylthio)- or US20240166618, Compound 26) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

Stereochemistry

(RS)-2,5-Dimethoxy-4-phenylthioamphetamine is a racemic mixture of the optical stereoisomers

See also

References

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 44719475, 2,5-Dimethoxy-4-phenylthioamphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/44719475.

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-phenylthioamphetamine. UNII: 3961V7J60A. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/3961V7J60A